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17447-84-6

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17447-84-6 Usage

General Description

9-BENZYL-(9H)-PURINE-6(1H)-THIONE is a chemical compound that belongs to the purine family and contains a benzyl group and a thione group. It is a derivative of purine and is frequently used as a building block in organic synthesis. 9-BENZYL-(9H)-PURINE-6(1H)-THIONE has potential biological activity and is being studied for its possible therapeutic uses in various diseases, including cancer and inflammatory disorders. Its structure gives it the potential to interact with biological targets, making it a valuable compound for research and drug development. Additionally, it has been reported to have antioxidant and antimicrobial properties, adding to its potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 17447-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,4 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17447-84:
(7*1)+(6*7)+(5*4)+(4*4)+(3*7)+(2*8)+(1*4)=126
126 % 10 = 6
So 17447-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N4S/c17-12-10-11(13-7-14-12)16(8-15-10)6-9-4-2-1-3-5-9/h1-5,7-8H,6H2,(H,13,14,17)

17447-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-benzyl-3H-purine-6-thione

1.2 Other means of identification

Product number -
Other names 9-benzyl-3,9-dihydro-6H-purine-6-thione

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:17447-84-6 SDS

17447-84-6Relevant articles and documents

Chemoselective Perfluoromethylation of Thio- And Selenoamides

Xu, Tao,Xu, Xianhong,Zhang, Jianyu

supporting information, (2020/11/13)

A chemo- and regioselective perfluoromethylation using thioamides/selenoamides (prepared one step from corresponding lactams) as starting materials has been discovered. The reaction demonstrated complementary chemoselectivity to the C-H trifluoromethylation of (hetero)arenes as well as remarkable functional group compatibility especially toward radical sensitive olefin-, alkyne-, and arylhalide-bearing substrates. The examples of perfluorothio-/selenolated drug molecules indicated application potential of this strategy in drug modification and drug-analogue preparation.

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