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5069-82-9

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5069-82-9 Usage

General Description

6-(butylthio)-purine is a chemical compound with the molecular formula C11H14N4S. It is a purine derivative that is often used as a research tool in biochemistry and pharmacology. 6-(BUTYLTHIO)-PURINE has a butylthio group attached to the purine ring, which can affect its pharmacological properties and activity. It is commonly used in studies related to adenosine receptors, as well as in the development of novel drugs for various medical conditions. The exact biological and pharmacological effects of 6-(butylthio)-purine are still being explored, but it shows potential as a valuable tool in scientific research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 5069-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5069-82:
(6*5)+(5*0)+(4*6)+(3*9)+(2*8)+(1*2)=99
99 % 10 = 9
So 5069-82-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N4S/c1-2-3-4-14-9-7-8(11-5-10-7)12-6-13-9/h5-7H,2-4H2,1H3

5069-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-butylsulfanyl-7H-purine

1.2 Other means of identification

Product number -
Other names SRI 712

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:5069-82-9 SDS

5069-82-9Downstream Products

5069-82-9Relevant articles and documents

Modification of thionucleobases in ionic liquids

Hu, Xiaomei,Zhang, Bixian,Dong, Shijia,Gao, Yunfei

, (2015/02/19)

A simple method was established for the preparation of thio-substituted thionucleobases using room temperature ionic liquids (RTILs) such as 1-butyl-3-methylimidazolium trifluoroacetate [BMIM]+[CF3COO]- and 1-methoxyethyl-3-methylimidazolium trifluoroacetate [MeOEtMIM]+[CF3COO]- as solvents and catalysts without any other catalyst. These reactions proceeded efficiently in RTILs with excellent yield of products. RTILs can be recycled and reused effectively without further purification.

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