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19850-47-6

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19850-47-6 Usage

Functional Groups

Hydrazinecarbothioamide
Trifluoromethyl
Indol-3-yl

Potential Biological Activities

Inhibitor of c-Src Enzyme: Involved in regulating cell growth and proliferation.
Anti-cancer Properties: Potential use in developing anti-cancer drugs.
Anti-inflammatory: May possess anti-inflammatory properties.
Antioxidant: Potential antioxidant properties.

Biomedical Applications

Promising candidate for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 19850-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,5 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19850-47:
(7*1)+(6*9)+(5*8)+(4*5)+(3*0)+(2*4)+(1*7)=136
136 % 10 = 6
So 19850-47-6 is a valid CAS Registry Number.

19850-47-6SDS

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 [[2-oxo-4-(trifluoromethyl)indol-3-yl]amino]thiourea

1.2 Other means of identification

Product number -
Other names -

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:19850-47-6 SDS

19850-47-6Downstream Products

19850-47-6Relevant articles and documents

Condensed heterocyclic systems containing bridgehead nitrogen atom: Synthesis and bioactivity of thiazolo[3′,2′:2,3][1,2,4]triazino[5,6-b]indole and isomeric thiazolo[2′,3′:3,4][1,2,4]triazin[5,6-b]indole

Mohan, Jag,Kataria, Sangeeta

, p. 456 - 458 (2007/10/03)

9-Trifluoromethyl-5H-2,3-dihydro[1,2,4]triazino[5,6-b]indole-3-thione (2) on condensation with p-chlorophenacylbromide gives 5H-3-p-chlorophenacylmercapto-9-trifluoromethyl[1,2,4]triazino-[5,6-b] indole hydrobromide (3) which on cyclization yields 3-p-chlorophenyl-6-trifluoromethyl-thiazolo[3′,2′:2,3][1,2,4] triazino[5,6-b]indole (4) and not the angular isomeric 1-(p-chlorophenyl)-6-trifluoromethylthiazolo[2′,3′:3,4][1,2,4] triazino[5,6-b]indole (6). The unequivocal synthesis of 6 has also been accomplished. The antibacterial and antifungal activity of 4 and 6 have been evaluated.

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