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9H-Purine, 6-chloro-9-[(1R,4S)-4-[nitro(phenylsulfonyl)methyl]-2-cyclopenten-1-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

188907-60-0

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188907-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188907-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,9,0 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 188907-60:
(8*1)+(7*8)+(6*8)+(5*9)+(4*0)+(3*7)+(2*6)+(1*0)=190
190 % 10 = 0
So 188907-60-0 is a valid CAS Registry Number.

188907-60-0SDS

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 (1'R,4'S)-1'-(6-chloropurin-9-yl)-4'-phenylsulfonyl(nitro)methyl-cyclopent-2'-ene

1.2 Other means of identification

Product number -
Other names 9-[(1R,4S)-4-(Benzenesulfonyl-nitro-methyl)-cyclopent-2-enyl]-6-chloro-9H-purine

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:188907-60-0 SDS

188907-60-0Relevant academic research and scientific papers

Palladium-catalyzed enantioselective synthesis of carbanucleosides

Trost, Barry M.,Madsen, Robert,Guile, Simon D.,Brown, Brian

, p. 5947 - 5956 (2007/10/03)

A general strategy has been developed for enantioselective synthesis of diverse carbanucleosides. The key step is a Pd(0)-catalyzed enantioselective allylic amination of cis-3,5-dibenzoyloxycyclopent-2-ene 10a with the nucleobase. With guanine-derived nuc

An enantio- and diastereo-controlled synthesis of (-)neplanocin A and its 2,3-di-epi isomer

Trost, Barry M.,Madsen, Robert,Guile, Simon D.

, p. 1707 - 1710 (2007/10/03)

An enantioselective Pd catalyzed desymmetrization of cis-3,5-dibenzoyloxycyclopent-2-ene combined with a diastereoselective epoxidation provided a common intermediate that can bifurcate to form either (-)-neplanocin A or its 2,3-di-epi isomer.

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