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Adenosine, 2'-deoxy-, 5'-benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90362-50-8

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90362-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90362-50-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,6 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90362-50:
(7*9)+(6*0)+(5*3)+(4*6)+(3*2)+(2*5)+(1*0)=118
118 % 10 = 8
So 90362-50-8 is a valid CAS Registry Number.

90362-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Adenosine, 2'-deoxy-, 5'-benzoate

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:90362-50-8 SDS

90362-50-8Relevant academic research and scientific papers

5′-O-Masked 2′-deoxyadenosine analogues as lead compounds for hepatitis C virus (HCV) therapeutic agents

Ikejiri, Masahiro,Ohshima, Takayuki,Kato, Keizo,Toyama, Masaaki,Murata, Takayuki,Shimotohno, Kunitada,Maruyama, Tokumi

, p. 6882 - 6892 (2008/04/12)

On the basis of our previous study on antiviral agents against the severe acute respiratory syndrome (SARS) coronavirus, a series of nucleoside analogues whose 5′-hydroxyl groups are masked by various protective groups such as carboxylate, sulfonate, and

ADA-Bypass by lipophilic cycloSal-ddAMP pro-nucleotides. A second example of the efficiency of the cycloSal-concept

Meier, Chris,Knispel, Tina,De Clercq,Balzarini, Jan

, p. 1577 - 1582 (2007/10/03)

The synthesis of lipophilic pro-nucleotides of ddAMP 2 based on cycloSal-ddAMP 3a-c is described. Phosphotriesters 3 released ddAMP 2 selectively by a controlled, chemically induced tandem reaction. CycloSal-phosphotriesters 3 exhibited antiviral activity against HIV-1/HIV-2 in CEM cells that where by a factor up to hundred higher as compared to ddA 1.

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