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17447-84-6

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17447-84-6 Usage

Description

9-BENZYL-(9H)-PURINE-6(1H)-THIONE is a purine derivative featuring a benzyl group and a thione group. It is a member of the purine family of compounds, which are essential in various biological processes. This chemical compound is recognized for its potential biological activity and is under investigation for its therapeutic potential in treating diseases such as cancer and inflammatory disorders. Its unique structure allows it to engage with biological targets, making it a significant compound for research and pharmaceutical development. Furthermore, it has been noted for its antioxidant and antimicrobial properties, which broaden its scope for application across different fields.

Uses

Used in Pharmaceutical Research and Development:
9-BENZYL-(9H)-PURINE-6(1H)-THIONE is utilized as a building block in organic synthesis for the development of new pharmaceuticals. Its potential biological activity makes it a candidate for therapeutic uses in various diseases, particularly in the areas of cancer and inflammatory disorders.
Used in Anticancer Applications:
In the field of oncology, 9-BENZYL-(9H)-PURINE-6(1H)-THIONE is studied for its possible role in cancer treatment. Its interaction with biological targets could contribute to the inhibition of cancer cell growth and the modulation of disease progression.
Used in Inflammatory Disorder Treatment:
9-BENZYL-(9H)-PURINE-6(1H)-THIONE is also being explored for its potential in managing inflammatory disorders, where its structure may help in reducing inflammation and associated symptoms.
Used in Antioxidant Formulations:
Given its antioxidant properties, 9-BENZYL-(9H)-PURINE-6(1H)-THIONE is considered for use in formulations that aim to protect cells from oxidative damage, which is a common factor in many diseases.
Used in Antimicrobial Agents:
The antimicrobial properties of 9-BENZYL-(9H)-PURINE-6(1H)-THIONE make it a potential candidate for the development of new antimicrobial agents, which could be used in various applications to combat microbial infections.
Used in Chemical Synthesis Industry:
As a building block in organic synthesis, 9-BENZYL-(9H)-PURINE-6(1H)-THIONE is used in the chemical synthesis industry to create a variety of compounds for different applications, including pharmaceuticals, agrochemicals, and other specialty chemicals.

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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