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7-DEAZA-2'-DEOXYXANTHOSINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96022-82-1

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96022-82-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96022-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,2 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96022-82:
(7*9)+(6*6)+(5*0)+(4*2)+(3*2)+(2*8)+(1*2)=131
131 % 10 = 1
So 96022-82-1 is a valid CAS Registry Number.

96022-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-pyrrolo[2,3-d]pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 7-Deaza-2'-deoxyxanthosine

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:96022-82-1 SDS

96022-82-1Downstream Products

96022-82-1Relevant academic research and scientific papers

Enhanced triple-helix and double-helix formation with oligomers containing modified purines

-

, (2008/06/13)

Novel oligomers are disclosed which have enhanced ability with respect to forming duplexes or triplexes compared with oligomers containing only conventional bases. The oligomers contain 7-deaza-7-substituted purines or related analogs. The oligomers of the invention are capable of (i) forming triplexes with various target sequences such as virus or oncogene sequences by coupling into the major groove of a target DNA duplex at physiological pH or (ii) forming duplexes by binding to single-stranded DNA or to RNA encoded by target genes. The oligomers of the invention can be constructed to have any desired sequence, provided the sequence normally includes one or more bases that is replaced with the analogs of the invention. Compositions of the invention can be used for diagnostic purposes in order to detect viruses or disease conditions.

7-Deaza Isosters of 2'-Deoxyxanthosine and 2'-Deoxyspongosine - Synthesis via Glycosylation of 2,4-Dichloro-7H-pyrrolopyrimidine

Seela, Frank,Driller, Hansjuergen,Liman, Ulrich

, p. 312 - 320 (2007/10/02)

7-Deaza-2'-deoxyxanthosine (1a) and 7-deaza-2'-deoxyspongosine (2), two new pyrrolopyrimidine deoxynucleosides, have been prepared by nucleophilic displacement of the chloro substituents of the intermediate 2,4-dichloro-7-2-deoxy-3,5-di-O-(p-toluo

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