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[3-(6-amino-9H-purin-9-yl)cyclobutyl]methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125962-36-9

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125962-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125962-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,6 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125962-36:
(8*1)+(7*2)+(6*5)+(5*9)+(4*6)+(3*2)+(2*3)+(1*6)=139
139 % 10 = 9
So 125962-36-9 is a valid CAS Registry Number.

125962-36-9SDS

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 3β-(6-amino-9H-purin-9-yl)cyclobutane-1β-methanol

1.2 Other means of identification

Product number -
Other names 9-<cis-3(hydroxymethyl)cyclobutyl>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:125962-36-9 SDS

125962-36-9Downstream Products

125962-36-9Relevant academic research and scientific papers

Synthesis of 9--adenine and -guanine

Kaiwar, Vijay,Reese, Colin B.,Gray, Emily J.,Neidle, Stephen

, p. 2281 - 2288 (2007/10/02)

2,2-Dichloro-3-(benzyloxymethyl)cyclobutanone 15, which was prepared in 50percent yield by the cycloaddition of dichloroketene to allyl benzyl ether 14, was converted in four steps and in ca. 40percent overall yield into trans-3-(benzyloxymethyl)cyclobutanol 11b.The latter alcohol 11b was coupled under Mitsunobu conditions with 6-(4-chlorophenylsulfanyl)-9H-purine 21b and 6-(4-chlorophenylsulfanyl)-2-(phenylacetamido)-9H-purine 21c to give the 9-cyclobutylpurine derivatives 22 and 24, respectively, in 88 and 60percent yield.The former product 22 was converted in three steps and in 39percent overall yield into 9-adenine 6, and the latter product was converted in four steps and in 42percent overall yield into 9-guanine 7.X-Ray crystallographic data relating to compounds 22 and 24 are also reported.

Novel cyclobutane Derivatives, processes for their preparation and pharmaceutical compositions comprising them

-

, (2008/06/13)

The invention is directed to cyclobutane derivatives represented by general formula (I): wherein A represents a hydrogen atom, a hydroxy group, an azido group or an amino group; and B represents a purine residue or a pyrimidine residue. The cyclobutane de

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