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88-11-9

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88-11-9 Usage

Description

Diethylthiocarbamoyl chloride, also known as N,N′-Diethylthiocarbamoyl chloride, is an organic compound that serves as a versatile synthetic intermediate in various chemical reactions and synthesis processes. It is characterized by its ability to form thiocarbamate derivatives, which are important in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.

Uses

Used in Pharmaceutical Synthesis:
Diethylthiocarbamoyl chloride is used as a synthetic intermediate for the production of aryl isothiocyanates, which are key compounds in the development of pharmaceuticals with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, Diethylthiocarbamoyl chloride is utilized as a synthetic intermediate for the synthesis of 5-substituted 4-methyl-2-thiazolyl diethyldithiocarbamates. These compounds exhibit pesticidal properties and are used in the development of effective and environmentally friendly crop protection agents.
Used in the Development of Novel Vasorelaxant Hybrid Compounds:
Diethylthiocarbamoyl chloride is employed as a synthetic intermediate in the creation of novel vasorelaxant hybrid compounds. These compounds have the potential to improve cardiovascular health by promoting the relaxation of blood vessels, thus reducing blood pressure and improving blood flow.
Used as a General Synthetic Intermediate:
Diethylthiocarbamoyl chloride is a valuable synthetic intermediate in various chemical reactions, enabling the synthesis of a wide range of organic compounds for use in different industries, including pharmaceuticals, agrochemicals, and specialty chemicals. Its versatility and reactivity make it an essential component in the development of new and innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 88-11-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88-11:
(4*8)+(3*8)+(2*1)+(1*1)=59
59 % 10 = 9
So 88-11-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H10ClNS/c1-3-7(4-2)5(6)8/h3-4H2,1-2H3

88-11-9 Well-known Company Product Price

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  • Aldrich

  • (384291)  Diethylthiocarbamoylchloride  95%

  • 88-11-9

  • 384291-5G

  • 947.70CNY

  • Detail
  • Aldrich

  • (384291)  Diethylthiocarbamoylchloride  95%

  • 88-11-9

  • 384291-25G

  • 3,229.20CNY

  • Detail

88-11-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diethylcarbamothioyl chloride

1.2 Other means of identification

Product number -
Other names Carbamothioic chloride, diethyl-

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:88-11-9 SDS

88-11-9Relevant articles and documents

Synthesis of Carbamic Esters Derivatives of Itols: Antifungal Activity against Various Crop Diseases

Len, Christophe,Postel, Denis,Ronco, Gino,Villa, Pierre,Goubert, Christel,Jeufrault, Eric,Mathon, Bernard,Simon, Herve

, p. 3 - 6 (1997)

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Method for preparing substituted thiophenol and heterocyclic thiophenol by continuous flow reactor

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Paragraph 0045-0047; 0051-0053; 0057-0059; 0063-0095, (2019/01/14)

The invention relates to a method for preparing substituted thiophenol and heterocyclic thiophenol by a continuous flow reactor. Phenol and phenol derivatives or heterocyclic phenol are taken as starting materials, and target compounds are prepared by four-step reactions of chlorination, esterification, rearrangement and hydrolysis, wherein the rearrangement reaction is conducted in the continuousflow reactor. According to the method, the reaction is guaranteed by a miniaturized heating device for high-temperature reaction and heat generated by the reaction, the conversion rate and the yieldhigher than those in the conventional reactor are obtained in the short residence time of tens of seconds, relevant side reactions are reduced, meanwhile, fluctuation of temperature and concentrationis avoided in the reaction process, temperature run-away and overheat are avoided, and the reaction process is safe and controllable.

SYNTHESIS OF N,N-DIALKYLCHLOROTHIOFORMAMIDES AND THEIR REACTIONS WITH PHOSPHOROUS ACID ESTERS

Pudovik, A. N.,Khairullin, V. K.,Vasyanina, M. A.

, p. 1328 - 1331 (2007/10/02)

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