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

162356-20-9

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162356-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162356-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,5 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 162356-20:
(8*1)+(7*6)+(6*2)+(5*3)+(4*5)+(3*6)+(2*2)+(1*0)=119
119 % 10 = 9
So 162356-20-9 is a valid CAS Registry Number.

162356-20-9Relevant academic research and scientific papers

Synthesis of Chiral Bicyclic Lactams Using Ring Closure Metathesis: Synthesis of (-)-Coniceine and (S)-Pyrrolam A

Arisawa, Mitsuhiro,Takezawa, Emiko,Nishida, Atsushi,Mori, Miwako,Nakagawa, Masako

, p. 1179 - 1180 (1997)

Chiral (-)-coniceine and (S)-pyrrolam A were synthesized from dienes prepared from L-proline by ring closure metathesis.

Benzotriazole-Mediated Stereoselective Olefination of Carboxylic Esters: Transformation of α-Amino Acid Esters into Chiral Allylamines

Katritzky, Alan R.,Cheng, Dai,Li, Jianqing

, p. 3438 - 3444 (2007/10/03)

Diastereoselective trans-olefinations of carboxylic esters 3a-h have been accomplished using benzylic or allylic benzotriazole derivatives 1a-e to prepare α-(benzotriazol-1-yl) ketones 4a-i, for the subsequent reduction of 4a-i, and finally for low-valent titanium-effected dehydroxybenzotriazolylation.1 N-Protected α-amino acid esters 9a-c and 15 thus give allylamines 13a-e and 19 with virtually full retention of chirality. Mechanistic aspects of the dehydroxybenzotriazolylation are discussed.

Stereochemical consequences of the Lewis acid-promoted 3-aza-cope rearrangement of N-alkyl-N-allyl enamines

Cook, Ggregory R.,Stille, John R.

, p. 4105 - 4124 (2007/10/02)

Internal and relative asymmetric induction were examined for the electrophile promoted 3-aza-Cope rearrangement of substituted N-alkyl-N-allyl enamines. In general, internal asymmetric induction was highly variable, and was dependent both upon the nature

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