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9-pentofuranosyl-8-(piperidin-1-yl)-9H-purin-6-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65456-86-2

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65456-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65456-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,5 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65456-86:
(7*6)+(6*5)+(5*4)+(4*5)+(3*6)+(2*8)+(1*6)=152
152 % 10 = 2
So 65456-86-2 is a valid CAS Registry Number.

65456-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-amino-8-piperidin-1-ylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

1.2 Other means of identification

Product number -
Other names 8-piperidin-1-yl-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:65456-86-2 SDS

65456-86-2Downstream Products

65456-86-2Relevant academic research and scientific papers

Anti-HCV nucleoside derivatives

-

, (2008/06/13)

The present invention comprises novel and known purine and pyrimidine nucleoside derivatives which have been discovered to be active against hepatitis C virus (HCV). The use of these derivatives for the treatment of HCV infection is claimed as are the novel nucleoside derivatives disclosed herein.

Synthesis and structure-activity relationships of adenosine analogs as inhibitors of trypanosomal glyceraldehyde-3-phosphate dehydrogenase. Modifications at positions 5' and 8

Aronov, Alex M.,Gelb, Michael H.

, p. 3505 - 3510 (2007/10/03)

A number of 5', N6- and C8, N6-disubstituted adenosine analogs was synthesized and tested for inhibition of trypanosomal glyceraldehyde 3- phosphate dehydrogenase. The most active compound, N6-(3-methyl-2-buteny

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