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68715-65-1

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68715-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68715-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,7,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68715-65:
(7*6)+(6*8)+(5*7)+(4*1)+(3*5)+(2*6)+(1*5)=161
161 % 10 = 1
So 68715-65-1 is a valid CAS Registry Number.

68715-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names -

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:68715-65-1 SDS

68715-65-1Downstream Products

68715-65-1Relevant articles and documents

6-Iodopurine as a Versatile Building Block for RNA Purine Architecture Modifications

Chen, Kun,Fang, Zhentian,He, Zhiyong,Heng, Panpan,Wang, Baoshan,Xie, Yalun,Yang, Wei,Zhou, Xiang

, p. 353 - 362 (2022/02/17)

Natural modified bases in RNA were found to be indispensable for basic biological processes. In addition, artificial RNA modifications have been a versatile toolbox for the study of RNA interference, structure, and dynamics. Here, we present a chemical method for the facile synthesis of RNA containing C6-modified purine. 6-Iodopurine, as a postsynthetic building block with high reactivity, was used for metal-free construction of C-N, C-O, and C-S bonds under mild conditions and C-C bond formation by Suzuki-Miyaura cross-coupling. Our strategy provides a convenient approach for the synthesis of various RNA modifications, especially for oligonucleotides containing specific structures.

Anti-malarial activity of N6-modified purine analogues

Too, Kathleen,Brown, Daniel M.,Bongard, Emily,Yardley, Vanessa,Vivas, Livia,Loakes, David

, p. 5551 - 5562 (2008/03/14)

Plasmodium falciparum causes one of the deadliest forms of malaria and resistance to the currently available drugs makes it imperative to develop new, safe and potent drugs. Parasites such as P. falciparum are unable to synthesise purines de novo and to t

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