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Cyclopentanecarboxaldehyde, 2-(2-oxo-2-phenylethyl)-, (1S,2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

871468-89-2

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871468-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 871468-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,4,6 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 871468-89:
(8*8)+(7*7)+(6*1)+(5*4)+(4*6)+(3*8)+(2*8)+(1*9)=212
212 % 10 = 2
So 871468-89-2 is a valid CAS Registry Number.

871468-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2S)-2-phenacylcyclopentane-1-carbaldehyde

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:871468-89-2 SDS

871468-89-2Relevant academic research and scientific papers

Asymmetric intramolecular Michael reaction catalyzed by proline-derived small anilides

Kikuchi, Makoto,Inagaki, Tomohiko,Nishiyama, Hisao

, p. 1075 - 1078 (2008/02/13)

Simple proline-derived anilide-catalyzed asymmetric intramolecular Michael reaction was described. Chiral cyclic ketoaldehydes were obtained from acyclic formyl enones in excellent yields with good stereoselectivity. The reaction proceeded in exceptionall

Catalytic asymmetric reductive Michael cyclization

Yang, Jung Woon,Hechavarria Fonseca, Maria T.,List, Benjamin

, p. 15036 - 15037 (2007/10/03)

A highly efficient and chemo-, regio-, diastereo-, and enantioselective organocatalytic tandem conjugate reduction-Michael cyclization of enal enones has been developed. Accordingly, treating the enal enone with a Hantzsch dihydropyridine in the presence

Cysteine-derived organocatalyst in a highly enantioselective intramolecular Michael reaction

Hayashi, Yujiro,Gotoh, Hiroaki,Tamura, Tomohiro,Yamaguchi, Hirofumi,Masui, Ryouhei,Shoji, Mitsuru

, p. 16028 - 16029 (2007/10/03)

Asymmetric intramolecular Michael reaction catalyzed by an organocatalyst derived from cysteine has been developed for the synthesis of chiral bicyclo[4.3.0]nonene and cis-disubstituted cyclopentane skeletons with a creation of three or two contiguous chiral centers in good yield with high diastereo- and excellent enantioselectivities. Copyright

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