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1007-51-8

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1007-51-8 Usage

Description

2-phenylhydrazinecarbodithioic acid, also known as phenylhydrazinecarbodithioic acid, is a chemical compound belonging to the class of carbodithioic acids. It is derived from hydrazine and features a phenyl group attached to the hydrazine nitrogen atom. 2-phenylhydrazinecarbodithioic acid has been studied for its potential therapeutic applications in treating various diseases, including cancer and viral infections. Its chemical properties and biological activities have garnered interest in pharmaceutical research and drug development. However, due to its toxicity and potential health hazards, the use and handling of 2-phenylhydrazinecarbodithioic acid require caution and appropriate safety measures.

Uses

Used in Pharmaceutical Research and Drug Development:
2-phenylhydrazinecarbodithioic acid is used as a subject of interest in pharmaceutical research and drug development for its potential use in treating various diseases, such as cancer and viral infections. Its unique chemical properties and biological activities make it a promising candidate for further investigation and development.
Used in Cancer Treatment:
2-phenylhydrazinecarbodithioic acid is used as a potential therapeutic agent in cancer treatment. Its chemical properties and biological activities have shown promise in targeting and treating various types of cancer. However, further research is needed to fully understand its mechanism of action and potential side effects.
Used in Viral Infection Treatment:
2-phenylhydrazinecarbodithioic acid is used as a potential therapeutic agent in the treatment of viral infections. Its unique chemical properties and biological activities have shown potential in targeting and inhibiting the replication of certain viruses. Further research is required to explore its efficacy and safety in treating viral infections.
Used in Chemical Synthesis:
2-phenylhydrazinecarbodithioic acid is used as a chemical intermediate in the synthesis of various compounds. Its unique structure and reactivity make it a valuable building block in the development of new chemical entities with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1007-51-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1007-51:
(6*1)+(5*0)+(4*0)+(3*7)+(2*5)+(1*1)=38
38 % 10 = 8
So 1007-51-8 is a valid CAS Registry Number.

1007-51-8SDS

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 potassium,anilinocarbamodithioic acid

1.2 Other means of identification

Product number -
Other names potassium phenyldithiocarbazate

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:1007-51-8 SDS

1007-51-8Relevant articles and documents

Synthesis and antimicrobial activity of new thiazole-2(3H)-thiones containing 1,1,3-trisubstituted cyclobutane

Ahmedzade, Misir,Kirilmis, Cumhur,Cukurovali, Alaaddin,Dilsiz, Nihat

, p. 21 - 24 (2007/10/03)

The reaction of potassium salts of RNHCSSK with 2-chloro-1-(3-methyl-3- phenylcyclobutyl)ethan-1-one in ethanol at 78-80°C afforded new 1,3-thiazole-2(3H)-thiones containing 1,1,3-trisubstituted cyclobutane rings at C-4. The antimicrobial activities of these compounds were also investigated against seven different microorganisms, and some of them were found to be active against several of the microorganisms at higher concentrations.

NOVEL REARRANGEMENT OF 3-AMINO-1,3-THIAZOLE-2-THIONE

Katritzky, Alan R.,Bayyuk, Shibli

, p. 3099 - 3106 (2007/10/02)

Some new derivatives of 3-amino- and 3-phenylamino-4-phenyl-1,3-thiazole-2-thione have been prepared and characterized.When 3-(N-phenylbenamido)-4-phenyl-1,3-thiazole-2-thione is rearranged thermally it gives 3-(2-benzoylphenylamino)-4-phenyl-1,3-thiazole

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