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5-(6-amino-9H-purin-9-yl)pentane-1,3-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69895-62-1

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69895-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69895-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,9 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69895-62:
(7*6)+(6*9)+(5*8)+(4*9)+(3*5)+(2*6)+(1*2)=201
201 % 10 = 1
So 69895-62-1 is a valid CAS Registry Number.

69895-62-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(6-aminopurin-9-yl)pentane-1,3-diol

1.2 Other means of identification

Product number -
Other names 9-(3,5-DiOHPentyl)Adenine

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:69895-62-1 SDS

69895-62-1Downstream Products

69895-62-1Relevant academic research and scientific papers

Synthesis of New (+/-)-3,5-Dihydroxypentyl Nucleoside Analogues from 1-Amino-5-(benzyloxy)pentan-3-ol and Their Antiviral Evaluation

Legraverend, Michel,Boumchita, Hassane,Zerial, Aurelio,Huel, Christiane,Lemaitre, Marc,Bisagni, Emile

, p. 2476 - 2480 (2007/10/02)

The synthesis and antiviral evaluation of a series of (+/-)-3,5-dihydroxypentyl nucleoside analogues related to acyclic nucleoside antiviral agents are reported.All purine and pyrimidine nucleoside analogues described in this paper have been obtained from 1-amino-5-(benzyloxy)pentan-3-ol.A synthesis of this amine is reported from 1-(benzyloxy)but-3-ene after epoxidation and regiospecific diethylaluminum chloride catalyzed opening of the epoxide by trimethylsilyl cyanide.The compounds were tested in vitro in infected MRC5 and CEM cells.None of the compounds exhibitedantiviral activity against HSV-1, HCMV, and HIV-1 with the exception of the guanine derivative 7, which inhibited the cytopathic effect of HSV-1 by 50percent at 12.5 μg/mL.

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