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6H-Purin-6-one, 2-amino-8-bromo-1,9-dihydro-9-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96412-45-2

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96412-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96412-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,1 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96412-45:
(7*9)+(6*6)+(5*4)+(4*1)+(3*2)+(2*4)+(1*5)=142
142 % 10 = 2
So 96412-45-2 is a valid CAS Registry Number.

96412-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-9-benzyl-8-bromo-3H-purin-6-one

1.2 Other means of identification

Product number -
Other names 6H-Purin-6-one,2-amino-8-bromo-1,9-dihydro-9-(phenylmethyl)

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:96412-45-2 SDS

96412-45-2Relevant academic research and scientific papers

Purine nucleoside analogues; 9: Benzylation of N2-acetyl-8- bromoguanine

Madre, Marina,Panchenko, Natella,Zhuk, Regina,Geenevasen, Jan A.,Van Den Burg, Alida,Koomen, Gerrit-Jan

, p. 775 - 778 (2007/10/03)

A one-step synthesis of regioisomeric N- and O-benzylated 8- bromoguanines 4, 5, 9, 10 via N2-acetyl-8-bromoguanine (2) is described. The possibility to prepare 8-oxo- and 8-chloroguanine derivatives 3, 11, 12 from the same compound 2 is demonstrated, 1H and 13C NMR spectra are used to locate the sites of aralkylation.

Annelation of Guanosine by Reaction with Methyl N-Cyanomethanimididate and Sodium Methoxide To Give a Tricyclic, Fluorescent Analogue of Adenosine

Agasimundin, Yankanagouda S.,Oakes, Fred T.,Kostuba, Linda J.,Leonard, Nelson J.

, p. 2468 - 2474 (2007/10/02)

A reagent consisting of methyl N-cyanomethanimidate and sodium methoxide in methanol converts guanosine to a fluorescent product, 8-amino-3,10-dihydro-10-oxo-3-β-D-ribofuranosyl-1,3,5-triazinopurine.The tricyclic N-ribonucleoside thus formed resemb

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