Welcome to LookChem.com Sign In|Join Free

CAS

  • or

102-08-9

Post Buying Request

102-08-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

102-08-9 Usage

Description

1,3-Diphenyl-2-thiourea, also known as N,N'-Diphenylthiourea, is an organic compound with the chemical formula C6H5NHCSNHC6H5. It is a white to off-white powder with a characteristic chemical structure that includes two phenyl rings connected to a thiourea group. 1,3-Diphenyl-2-thiourea exhibits a wide dipole moment, making it useful in various applications.

Uses

Used in Rubber Industry:
1,3-Diphenyl-2-thiourea is used as a vulcanizing accelerator and activator for chloroprene rubber and ethylene-propylene-diene terpolymers. It enhances the rubber's properties and improves its performance in various applications.
Used in Dye Industry:
1,3-Diphenyl-2-thiourea is used in the production of sulfur dyes, which are important for coloring textiles and other materials.
Used in Pharmaceutical Industry:
1,3-Diphenyl-2-thiourea is used as an intermediate for organic synthesis in the pharmaceutical industry, contributing to the development of new drugs and medicinal compounds.
Used in Mining Industry:
As a flotation agent, 1,3-Diphenyl-2-thiourea is employed in the mining industry for the selective separation of minerals, such as galena, nickel, and cobalt, from their ores.
Used in Chemical Industry:
1,3-Diphenyl-2-thiourea serves as an acid inhibitor and is used in the development of co-crystals for nonlinear optics, generating new coherent wavelengths.
Used in Radiopharmaceutical Imaging:
Due to its ability to form metal chelated complexes, 1,3-Diphenyl-2-thiourea is used in radiopharmaceutical imaging and for treating metal poisoning.
Used in Plastics Industry:
As a heat stabilizer, 1,3-Diphenyl-2-thiourea is used in PVC adhesive-tape backing to prevent thermal degradation and improve the product's performance.

Synthesis Reference(s)

Tetrahedron Letters, 15, p. 1191, 1974 DOI: 10.1016/S0040-4039(01)82442-4

Air & Water Reactions

Insoluble in water.

Reactivity Profile

An organosulfide amide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Health Hazard

ACUTE/CHRONIC HAZARDS: When heated to decomposition 1,3-Diphenyl-2-thiourea emits highly toxic fumes.

Fire Hazard

Flash point data for 1,3-Diphenyl-2-thiourea are not available. 1,3-Diphenyl-2-thiourea is probably combustible.

Flammability and Explosibility

Nonflammable

Contact allergens

It is a rubber chemical used as an accelerator and stabilizing agent in neoprene

Safety Profile

Moderately toxic by ingestion and intraperitoneal routes. Experimental reproductive effects. When heated to decomposition it emits highly toxic fumes of SOx, and NOx,.

Purification Methods

Crystallise the thiourea from boiling EtOH by adding hot water and allowing to cool. [Beilstein 12 H 394, 12 IV 810.]

Check Digit Verification of cas no

The CAS Registry Mumber 102-08-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102-08:
(5*1)+(4*0)+(3*2)+(2*0)+(1*8)=19
19 % 10 = 9
So 102-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2S/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15,16)

102-08-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (T0197)  1,3-Diphenyl-2-thiourea  

  • 102-08-9

  • 25g

  • 130.00CNY

  • Detail
  • TCI America

  • (T0197)  1,3-Diphenyl-2-thiourea  

  • 102-08-9

  • 500g

  • 325.00CNY

  • Detail
  • Alfa Aesar

  • (A19644)  N,N'-Diphenylthiourea, 98%   

  • 102-08-9

  • 100g

  • 201.0CNY

  • Detail
  • Alfa Aesar

  • (A19644)  N,N'-Diphenylthiourea, 98%   

  • 102-08-9

  • 500g

  • 340.0CNY

  • Detail
  • Alfa Aesar

  • (A19644)  N,N'-Diphenylthiourea, 98%   

  • 102-08-9

  • 2500g

  • 889.0CNY

  • Detail
  • Aldrich

  • (T28355)  N,N′-Diphenylthiourea  98%

  • 102-08-9

  • T28355-25G

  • 223.47CNY

  • Detail

102-08-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Diphenyl-2-thiourea

1.2 Other means of identification

Product number -
Other names Thiocarbanilide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:102-08-9 SDS

102-08-9Relevant articles and documents

Copper-Catalyzed Double Thiolation to Access Sulfur-Bridged Imidazopyridines with Isothiocyanate

Tian, Lu-Lu,Lu, Shuai,Zhang, Zhe-Hua,Huang, En-Ling,Yan, Hua-Ting,Zhu, Xinju,Hao, Xin-Qi,Song, Mao-Ping

, p. 5213 - 5221 (2019)

A copper(I)-catalyzed sulfur-bridged dimerization of imidazopyridines has been developed using isothiocyanate as the sulfur source. This method enables a switchable synthesis of bis(imidazo[1,2-a]pyridin-3-yl)sulfanes or bis(2-(imidazo[1,2-a]pyridin-2-yl)phenyl)sulfanes in the presence of 4-dimethylaminopyridine (DMAP) or K2CO3 when different imidazopyridines were employed. Under optimized conditions, a variety of sulfur-bridged imidazopyridines were obtained in good yields. Moreover, thiourea was proved to be the key intermediate under catalytic system A.

-

Chattopadhyaya,Rao

, p. 289 (1974)

-

Rapid synthesis of a 13C6-benzothiazolium salt from 13C6-aniline

Galliford, Chris V.,Voronin, Kimberly,Hesk, David,Koharski, David,McNamara, Paul

, p. 229 - 232 (2011)

13C6-labeled aniline was used as a starting material for the facile synthesis of 13C6-benzothiazolium salt (1). Copyright

Barbiturate squaraine dyes as fluorescent probes for serum albumins detection

Almeida, Paulo,Boto, Renato E. F.,Gomes, Vanessa S. D.,Gon?alves, Helena M. R.,Reis, Lucinda V.

, (2020)

Three indolenine-based barbiturate squaraine dyes were synthesized, characterized and subjected to photophysical studies, including their affinity with human serum albumin and bovine serum albumin as protein models in phosphate buffer solution. All dyes successfully interact with both proteins with high affinity binding constants. It was found that dyes with hydrophobic substituents had superior binding constants with both proteins. The fluorescence intensity of all dyes increased in the presence of both proteins which allowed the determination of detection and quantifications limits in the tens of nanomolar, using a protein concentration of 0–3.5 μM. Concerning to the study on the binding sites of the synthesized dyes using the warfarin and ibuprofen markers, the results of this study suggest that, one dye binds to both BSA binding sites while the two others dyes binds only to site I, and that all three dyes bind to both HSA binding sites.

-

Feuer,Braunstein

, p. 2024 (1969)

-

Structural requirement of phenylthiourea analogs for their inhibitory activity of melanogenesis and tyrosinase

Thanigaimalai, Pillaiyar,Lee, Ki-Cheul,Sharma, Vinay K.,Joo, Cheonik,Cho, Won-Jea,Roh, Eunmiri,Kim, Youngsoo,Jung, Sang-Hun

, p. 6824 - 6828 (2011)

Effect of a series of 1-phenylthioureas 1a-k and 1,3-disubstituted thioureas 2a-k were evaluated against melanin formation in melanoma B16 cell line and mushroom tyrosinase. Inhibitory activity of tyrosinase of 1-phenylthioureas 1a-k is parallel to their melanogenic inhibition. Thus, the melanogenic inhibition in melanoma B16 cells of 1-phenylthioureas could be the result of inhibition of tyrosinase. However, 1,3-diaryl or 1-phenyl-3- alkylthioureas, 2a-k, appears as melanogenic inhibitor without inhibition of tyrosinase. The molecular docking study of 1e and 2b to binding pocket of tyrosinase provided convincing explanation regarding the necessity of direct connection of planar phenyl to thiourea unit without N′-substitution of phenylthioureas 1 as tyrosinase inhibitor and 2 as non-tyrosinase inhibitor.

A CONVENIENT METHOD FOR THE PREPARATION OF N,N'-DISUBSTITUTED THIOUREAS USING 2-CHLOROPYRIDINIUM SALT, SODIUM TRITHIOCARBONATE AND AMINES

Takikawa, Yuji,Inoue, Noriyuki,Sato, Ryu,Takizawa, Saburo

, p. 641 - 642 (1982)

N,N'-Disubstituted thioureas were prepared in high yields by treating 2-chloropyridinium salt with sodium trithiocarbonate and subsequently adding amines.

-

Hodgkins,Reeves

, p. 3098 (1964)

-

A convenient route to substituted thiocarbamides

Ramadas,Srinivasan

, p. 3381 - 3387 (1995)

-

Unclicking of thioureas: Base catalyzed elimination of anilines and isothiocyanates from thioureas

Vlatkovi?, Matea,Feringa, Ben L.

, p. 2188 - 2192 (2019)

Bisaromatic thioureas are widely used in e.g. asymmetric organocatalysis and considered to be robust compounds. Herein we show, in strong contrast to common notion, that thioureas dissociate to amines and isothiocyanates in a base catalyzed reaction under mild conditions. This ‘unclicking’ process can occur in the presence of weak organic bases even at moderate temperatures. The influence of the substituents at the aromatic rings of the thiourea on the regioselectivity of this unclicking process is also shown.

A general and facile one-pot process of isothiocyanates from amines under aqueous conditions

Sun, Nan,Li, Bin,Shao, Jianping,Mo, Weimin,Hu, Baoxiang,Shen, Zhenlu,Hu, Xinquan

, p. 61 - 70 (2012)

A general and facile one-pot protocol for the preparation of a broad range of alkyl and aryl isothiocyanates has been developed from their corresponding primary amines under aqueous conditions. This synthetic process involves an in situ generation of a dithiocarbamate salt from the amine substrate by reacting with CS2 followed by elimination to form the isothiocyanate product with cyanuric acid as the desulfurylation reagent. The choice of solvent is of decisive importance for the successful formation of the dithiocarbamate salt particularly for highly electron-deficient substrates. This novel and economical method is suitable for scale-up activities.

Carbon tetrabromide promoted reaction of amines with carbon disulfide: Facile and efficient synthesis of thioureas and thiuram disulfides

Liang, Fushun,Tan, Jing,Piao, Chengri,Liu, Qun

, p. 3579 - 3584 (2008)

A novel carbon tetrabromide promoted one-pot reaction of amines and carbon disulfide under mild conditions has been developed, which provides a straightforward and efficient access to thioureas and thiuram disufides, depending on the nature of the amines employed. The promotion effect is explained as the transient formation of a sulfenyl bromide intermediate from dithiocarbamate and carbon tetrabromide during the reaction. Georg Thieme Verlag Stuttgart · New York.

-

Shahak,Sasson

, p. 3440 (1973)

-

Quantitative estimation of the α-effect in the reactions yielding phosphorus-containing thiosemicarbazides

Yanchuk

, p. 1240 - 1242 (2006)

The α-effect in the reactions of O,O-diaryl phosphorohydrazidothioates with phenyl isothiocyanate in benzene at 25°C was quantitatively evaluated from the kinetic data. The probable reaction mechanism was suggested, and the causes of the α-effect in these reactions are discussed. An approximate linear correlation is observed between the α-effect in the reactions of O,O-diaryl phosphorohydrazidothioates with phenyl isothiocyanate, basicity constants of the hydrazides, and σp constants of the substituents at the P atom. The value of the α-effect is largely determined by the structure of the transition state. Nauka/Interperiodica 2006.

-

Helgen et al.

, p. 884 (1959)

-

CuI-catalyzed sulfenylation of 1-aryl trifluoromethyl pyrazolones: Direct formation of C-S-C bond using aryl iodides and carbon disulfide

Avalani, Jemin R.,Kamani, Ronak D.,Prajapati, Ronak V.,Prajapati, Vaibhav D.,Purohit, Vishal B.,Raval, Dipak K.,Sapariya, Nirav H.

supporting information, (2021/11/20)

A novel approach for CuI-catalyzed sulfenylation of 1-aryl-3-trifluoromethyl pyrazolones (2a-d) with aryl iodides (1a-j) and carbon disulfide as sulfenylating agent has been described. The protocol was found to be simple and efficient benign to access a broad array of fluorinated sulfenyl pyrazolones in good yields. The formation of C-S-C bond was achieved by using inexpensive and readily available starting materials.

The coordination chemistry of sulfonyl-substituted thioureas towards the d8 metal centres platinum(II), palladium(II), nickel(II) and gold(III)

Henderson, William,Risi, Matthew C.,Saunders, Graham C.

, (2021/07/13)

Reactions of the complexes cis-[PtCl2(PPh3)2], [PtCl2(dppp)] (dppp = Ph2P(CH2)3PPh2), [MCl2(dppe)] (dppe = Ph2P(CH2)2PPh2, M = Ni, Pd), [PdCl2(bipy)] (bipy = 2,2′-bipyridine) and [AuCl2(bp)] (bp = cyclometallated 2-benzylpyridine) with p-TolSO2NHC(S)NHPh and Et3N in refluxing methanol gave a series of new thiourea complexes containing the ligand bound as a dianion through the S and the NPh groups. The related thioureas RSO2NHC(S)NHPh (R = Me, Et) and p-TolSO2NHC(S)NHCH2CH=CH2 were also reacted with cis-[PtCl2(PPh3)2] to form the corresponding complexes [Pt{RSO2NC(S)NPh}(PPh3)2] and [Pt{TolSO2NC(S)NCH2CH=CH2}(PPh3)2] respectively. X-ray structure determinations were carried out on the thiourea MeSO2NHC(S)NHPh and its platinum complex [Pt{MeSO2NC(S)NPh}(PPh3)2], as well as [Pt{TolSO2NC(S)NPh}(PPh3)2]. Both complexes form the distal isomer with a remote NSO2R group, and no evidence was observed for isomerisation of these platinum complexes in solution. The palladium complexes [Pd{TolSO2NC(S)NPh}L2] [L2 = Ph2PCH2CH2PPh2 (dppe), or 2,2′-bipyridine (bipy)] undergo decomposition in solution to form the sulfide-bridged aggregates [Pd3S2(L2)3]2+, identified by ESI MS and 31P NMR.

Identification of organophosphorus simulants for the development of next-generation detection technologies

Ellaby, Rebecca J.,Clark, Ewan R.,Allen, Nyasha,Taylor, Faith R.,Ng, Kendrick K. L.,Dimitrovski, Milan,Chu, Dominique F.,Mulvihill, Daniel P.,Hiscock, Jennifer R.

, p. 2008 - 2014 (2021/03/16)

Organophosphorus (OP) chemical warfare agents (CWAs) represent an ongoing threat but the understandable widespread prohibition of their use places limitations on the development of technologies to counter the effects of any OP CWA release. Herein, we describe new, accessible methods for the identification of appropriate molecular simulants to mimic the hydrogen bond accepting capacity of the PO moiety, common to every member of this class of CWAs. Using the predictive methodologies developed herein, we have identified OP CWA hydrogen bond acceptor simulants for soman and sarin. It is hoped that the effective use of these physical property specific simulants will aid future countermeasure developments.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 102-08-9