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9-butyl-6-(methylsulfanyl)-9H-purin-2-amine is a chemical compound with the molecular formula C10H16N6S. It is a derivative of purine, an important component of nucleic acids, and features a 9-butyl group, a 6-methylsulfanyl group, and a 2-amine group. 9-butyl-6-(methylsulfanyl)-9H-purin-2-amine is known for its potential applications in medicinal chemistry, particularly in the development of antiviral and anticancer drugs, as it can interfere with the synthesis of nucleic acids in viruses and cancer cells. Its structure and properties make it a subject of interest for researchers exploring new therapeutic strategies.

14666-87-6

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14666-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14666-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14666-87:
(7*1)+(6*4)+(5*6)+(4*6)+(3*6)+(2*8)+(1*7)=126
126 % 10 = 6
So 14666-87-6 is a valid CAS Registry Number.

14666-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-butyl-6-methylsulfanylpurin-2-amine

1.2 Other means of identification

Product number -
Other names 9-Butyl-2-amino-6-methylmercapto-9H-purin

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

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More Details:14666-87-6 SDS

14666-87-6Downstream Products

14666-87-6Relevant academic research and scientific papers

ALKYLATION OF 6-METHYLTHIO- AND 6-BENZYLOXYGUANINE UNDER PHASE-TRANSFER CONDITIONS

Ramzaeva, N.,Alksnis, E.,Goldberg, Yu.,Lidaks, M.

, p. 3121 - 3128 (2007/10/02)

Phase-transfer-catalyzed alkylation of 6-methylthio- and 6-benzyloxyguanine followed by acid hydrolysis provides a simple procedure for the preparation of various 9- and 7-substituted guanines.

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