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3H-Purin-6-amine, 3-methyl-N-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76227-28-6

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76227-28-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76227-28-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,2 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76227-28:
(7*7)+(6*6)+(5*2)+(4*2)+(3*7)+(2*2)+(1*8)=136
136 % 10 = 6
So 76227-28-6 is a valid CAS Registry Number.

76227-28-6SDS

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 3-methyl-N-phenylmethoxypurin-6-amine

1.2 Other means of identification

Product number -
Other names N6-benzyloxy-3-methyladenine

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:76227-28-6 SDS

76227-28-6Relevant academic research and scientific papers

Purines. XXIII. Synthesis of N6-Alkoxy-1,3-dialkyladeninium Salts and an Attempt to Synthesize 1,3-Dimethyladenine

Fujii, Tozo,Saito, Tohru,Nakasaka, Tsuyoshi

, p. 3521 - 3527 (2007/10/02)

Ethylation of N6-methoxy-3-methyladenine (5) with EtI in AcNMe2 gave the 1-ethylated product 8 (X=I) (21percent yield) and the N6-ethylated product 11 (X=ClO4) (33percent).The N6-benzyloxy analogue 6, prepared from 3-methy

Synthesis, Ring Opening, and Glycosidic Bond Cleavage of 3-Methyl-2'-deoxyadenosine

Fujii, Tozo,Saito, Tohru,Nakasaka, Tsuyoshi

, p. 758 - 759 (2007/10/02)

Methylation of N'-benzyloxy-1-(2-deoxy-β-D-ribofuranosyl)-5-formamidoimidazole-4-carboxamidine (2a) followed by hydrogenolysis of the N'-benzyloxy-group and cyclization produced the hitherto unknown 3-methyl-2'-deoxyadenosine (5a), which was readily hydrolysed to 3-methyladenine (6) in H2O at pH /=7.0 and to (6) and the imidazole-(2-deoxy)riboside (4a) at pH 8.98.

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