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Benzeneacetic acid, 4-fluoro-, 2-(aminothioxomethyl)hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39203-09-3

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39203-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39203-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,0 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39203-09:
(7*3)+(6*9)+(5*2)+(4*0)+(3*3)+(2*0)+(1*9)=103
103 % 10 = 3
So 39203-09-3 is a valid CAS Registry Number.

39203-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-fluorophenyl)acetyl]hydrazinecarbothioamide

1.2 Other means of identification

Product number -
Other names 1-[2-(4-Fluorphenyl)-acetyl]-3-thiosemicarbazid

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:39203-09-3 SDS

39203-09-3Upstream product

39203-09-3Relevant academic research and scientific papers

THIADIAZOLE DERIVATIVES, INHIBITORS OF STEAROYL-COA DESATURASE

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Page/Page column 56, (2008/12/07)

The present invention relates to substituted thiadiazole compounds of the formula (I) and pharmaceutically acceptable salts thereof, to pharmaceutical compositions containing them and their use in medicine. In particular, the invention relates to compounds for modulating SCD activity.

2-Amino-5-(substituted or unsubstituted phenylalkyl)-thiadiazoles

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, (2008/06/13)

2-amino-5-(substituted or unsubstituted phenylalkyl)-thiadiazoles, e.g., 2-amino-5-(4-[phenylbutyl])-thiadiazole, prepared, e.g., by ring closure, of corresponding 1-(substituted or unsubstituted phenylalkanoyl)-thiosemicarbazide in a strong acid medium.

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