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13020-83-2

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13020-83-2 Usage

General Description

Trimethyl(purin-6-yl)ammonium chloride is a chemical compound that consists of a purine derivative attached to a trimethylammonium chloride group. It is a quaternary ammonium salt with a purine core, making it a positively charged molecule. trimethyl(purin-6-yl)ammonium chloride has potential use as a biochemical agent, possibly for research purposes or therapeutic applications due to its unique structure and properties. However, further studies are needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 13020-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,2 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13020-83:
(7*1)+(6*3)+(5*0)+(4*2)+(3*0)+(2*8)+(1*3)=52
52 % 10 = 2
So 13020-83-2 is a valid CAS Registry Number.

13020-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(7H-purin-6-yl)azanium,chloride

1.2 Other means of identification

Product number -
Other names N6,N6,N6-trimethyladeninium chloride

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:13020-83-2 SDS

13020-83-2Downstream Products

13020-83-2Relevant articles and documents

The new convenient synthesis of 6-fluoropurine and its 7-/9-unsubstituted analogues

Deng, Mei,Wang, Ningyu,Xiang, Guangming,Yu, Luoting

, p. 2999 - 3006 (2012)

6-Fluoropurine and its 7-/9-unsubstituted analogues have good biological activity and serve as important pharmaceutical intermediates. This paper describes a new and convenient synthesis of 6-fluoropurine and its 7-/9-unsubstituted analogues, by first replacing the chlorine atoms with trimethylammonio groups through the reaction of 6-chloropurine and its 7-/9-unsubstituted analogues with trimethylamine, and then replacing the trimethylammonio groups with fluorine atoms using safe and cheap TBAF·3H2O as fluorinating agent at room temperature. Compared with reported methods, the new synthesis has milder conditions, shorter reaction times, simpler post-processing and higher (or similar) yields.

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