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9H-Purine-2,6-diamine, 9-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30720-65-1

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30720-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30720-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,2 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30720-65:
(7*3)+(6*0)+(5*7)+(4*2)+(3*0)+(2*6)+(1*5)=81
81 % 10 = 1
So 30720-65-1 is a valid CAS Registry Number.

30720-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-methylpurine-2,6-diamine

1.2 Other means of identification

Product number -
Other names 2-Amino-9-methyladenin

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:30720-65-1 SDS

30720-65-1Downstream Products

30720-65-1Relevant academic research and scientific papers

The 't-amino effect' of ortho-nitroso amines. Synthesis of 2,6-diaminoadenine derivatives from 6-(Dialkylamino)-5-nitrosopyrimidines

Del Carmen Ruiz, Maria,Vasella, Andrea

experimental part, p. 785 - 800 (2011/06/24)

The 't-amino effect' of amino-nitroso compounds was documented by preparing the (dialkylamino)-nitroso pyrimidines 4-18, and cyclising them under thermal conditions in high yields to the purine derivatives 19-32. The reactivity of the amino-nitroso-pyrimi

Tricyclic purine analogs derived from 2-amino-6-chloropurine and 2,6-diaminopurine and their methylated quaternary salts

Horejsi, Katerina,Pohl, Radek,Holy, Antonin

, p. 77 - 90 (2007/10/03)

A novel series of tricyclic, etheno-bridged purine analogs was sythesized from 2-amino-6-(substituted amino)-9-methylpurines by cyclization with chloroacetaldehyde, with particular focus on the regioselectivity of the cyclization reaction and fluorescence properties. The analogs as well as the starting purines were alkylated with iodomethane, affording a new class of quaternary salts with potential biological activity. Neither significant fluorescence nor cytostatic effect was found.

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