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N-(4-methoxyphenyl)-9-pentofuranosyl-9H-purin-6-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29204-77-1

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29204-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29204-77-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,0 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29204-77:
(7*2)+(6*9)+(5*2)+(4*0)+(3*4)+(2*7)+(1*7)=111
111 % 10 = 1
So 29204-77-1 is a valid CAS Registry Number.

29204-77-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(hydroxymethyl)-5-[6-(4-methoxyanilino)purin-9-yl]oxolane-3,4-diol

1.2 Other means of identification

Product number -
Other names N6-(p-Methoxyphenyl)adenosine

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:29204-77-1 SDS

29204-77-1Downstream Products

29204-77-1Relevant academic research and scientific papers

GPR103 protein receptor inhibitor as well as preparation and application thereof

-

Paragraph 0084; 0088, (2021/06/06)

The invention provides a GPR103 protein receptor inhibitor as well as preparation and application thereof, and particularly provides a compound shown as a formula I or pharmaceutically acceptable salt thereof. The compound has excellent GPR103 protein inhibitory activity.

A highly facile and efficient one-step synthesis of N6-adenosine and N6-2′-deoxyadenosine derivatives

Wan, Zhao-Kui,Binnun, Eva,Wilson, Douglas P.,Lee, Jinbo

, p. 5877 - 5880 (2007/10/03)

(Chemical Equation Presented) A highly facile and efficient one-step synthesis of N6-adenosine and N6-2′-deoxyadenosine derivatives has been developed. Treatment of inosine or 2′-deoxyinosine, without protection of sugar hydroxyl groups, with alkyl or arylamines, in the presence of BOP and DIPEA in DMF, led to the formation of N6- adenosine and N6-2′-deoxyadenosine derivatives in good to excellent yields. Carcinogenic polyaromatic hydrocarbon (PAH) N 6-2′-deoxyadenosine adduct 10 and a rare DNA constituent 11 were thus synthesized directly from 2′-deoxyinosine both in 98% yield.

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