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N(2)-phenyl-2'-deoxyguanosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114300-71-9

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114300-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114300-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,0 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 114300-71:
(8*1)+(7*1)+(6*4)+(5*3)+(4*0)+(3*0)+(2*7)+(1*1)=69
69 % 10 = 9
So 114300-71-9 is a valid CAS Registry Number.

114300-71-9SDS

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 N-Phenyl-9-(β-D-ribofuranosyl)-9H-purin-2-amine

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:114300-71-9 SDS

114300-71-9Downstream Products

114300-71-9Relevant academic research and scientific papers

Chemoselective Arylation of 2'-Deoxyguanosine at N-2 with Organoiron Complexes

Potter, Gerard A.,McCague, Raymond,Jarman, Michael

, p. 637 - 638 (2007/10/02)

2'-Deoxyguanosine has been directly and chemoselectively arylated at the N2-amino function by treatment with tricarbonyl(η5-cyclohexadienylium)iron or tricarbonyl5-2-(n-butyl)cyclohexadienylium>iron cations, followed by

N2-phenyldeoxyguanosine: a novel selective inhibitor of herpes simplex thymidine kinase.

Focher,Hildebrand,Freese,Ciarrocchi,Noonan,Sangalli,Brown,Spadari,Wright

, p. 1496 - 1500 (2007/10/02)

A series of N2-substituted guanine derivatives was screened against mammalian thymidine kinase and the thymidine kinase encoded by type I herpes simplex virus to examine their capacity to selectivity inhibit the viral enzyme. Several bases, nucleosides, a

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