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9-(2-deoxypentopyranosyl)-9H-purin-6-amine, also known as 2'-deoxyadenosine or dAdo, is a nucleoside composed of a purine base (adenine) attached to a 2'-deoxyribose sugar. 9-(2-deoxypentopyranosyl)-9H-purin-6-amine is a key component of DNA, where it pairs with thymidine (thymine) to form the base pairs that contribute to the double helix structure. It plays a crucial role in the storage and transmission of genetic information, as well as in various biochemical processes within cells. The absence of an oxygen atom at the 2' position of the sugar ring distinguishes it from adenosine, which is found in RNA. This modification is significant for the stability and function of DNA, and it also affects the interactions of dAdo with enzymes and other molecules within the cell.

7697-49-6

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7697-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7697-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,9 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7697-49:
(6*7)+(5*6)+(4*9)+(3*7)+(2*4)+(1*9)=146
146 % 10 = 6
So 7697-49-6 is a valid CAS Registry Number.

7697-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methylpurine-2'-deoxyriboside

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7697-49-6 SDS

7697-49-6Downstream Products

7697-49-6Relevant academic research and scientific papers

SnCl4 versus TiCl4-mediated coupling between N-6-benzoyladenine and perbenzoylated 2-deoxypyranose: Application to the synthesis of certain homochiral acyclo and carboacyclonucleosides

Baud, Marie-V.,Chavis, Claude,Lucas, Marc,Imbach, Jean-L.

, p. 9993 - 10002 (2007/10/02)

1,3,4-tri-O-benzoyl 2-deoxyribopyranose and persilylated N-6-benzoyladenine react in two different and regioselective ways according to the nature of the coupling reagent SnCl4 or TiCl4. The former Lewis acid gives rise to the anomer

Improved procedure for the regiospecific synthesis of 2'-deoxyribonucleosides

Baud,Chavis,Lucas,Imbach

, p. 4437 - 4440 (2007/10/02)

2'-Deoxyribonucleosides are regiospecifically synthesized in high yields by catalyzing with KI-dibenzo-18-crown-6 PTC the condensation between unprotected silylated purines and pyrimidines and the appropriate easily available 2-deoxy-ribofuranosyl or pyranosyl sugar derivatives.

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