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(2S,1μS, 2μS)-Pyrrolidine-2-carboxylic acid (2-hydroxy-1,2-diphenyl-ethyl)amide is a complex organic compound with a unique molecular structure. It is characterized by its chiral centers, which give it specific stereochemistry and potential for various applications in different industries.

529486-26-8

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529486-26-8 Usage

Uses

Used in Pharmaceutical Industry:
(2S,1μS, 2μS)-Pyrrolidine-2-carboxylic acid (2-hydroxy-1,2-diphenyl-ethyl)amide is used as a catalyst for the synthesis of α-hydroxyaminocarbonyl compounds. This application is due to its ability to facilitate the N-nitroso aldol reaction between aldehydes and nitrosobenzenes, leading to the formation of valuable intermediates in the pharmaceutical industry.
Used in Chemical Synthesis:
In the field of chemical synthesis, (2S,1μS, 2μS)-Pyrrolidine-2-carboxylic acid (2-hydroxy-1,2-diphenyl-ethyl)amide is used as a catalyst for direct aldol reactions. This involves the reaction of aldehydes with chloroacetones, methylthio-, and fluoroacetones. (2S,1μS, 2μS)-Pyrrolidine-2-carboxylic acid (2-hydroxy-1,2-diphenyl-ethyl)amide's catalytic properties enable the formation of important synthetic building blocks, which can be further utilized in the development of various chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 529486-26-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,9,4,8 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 529486-26:
(8*5)+(7*2)+(6*9)+(5*4)+(4*8)+(3*6)+(2*2)+(1*6)=188
188 % 10 = 8
So 529486-26-8 is a valid CAS Registry Number.

529486-26-8 Well-known Company Product Price

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  • Aldrich

  • (671193)  (2S)-N-[(1S,2S)-2-Hydroxy-1,2-diphenylethyl]-2-pyrrolidinecarboxamide  ≥99% (HPLC)

  • 529486-26-8

  • 671193-100MG

  • 851.76CNY

  • Detail
  • Aldrich

  • (671193)  (2S)-N-[(1S,2S)-2-Hydroxy-1,2-diphenylethyl]-2-pyrrolidinecarboxamide  ≥99% (HPLC)

  • 529486-26-8

  • 671193-500MG

  • 3,237.39CNY

  • Detail

529486-26-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-N-[(1S,2S)-2-hydroxy-1,2-diphenylethyl]pyrrolidine-2-carboxamide

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:529486-26-8 SDS

529486-26-8Downstream Products

529486-26-8Relevant academic research and scientific papers

Asymmetric conjugate addition of ketones to β-nitrostyrenes by means of 1,2-amino-alcohol-derived prolinamides as bifunctional catalysts

Almasi, Diana,Alonso, Diego A.,Gomez-Bengoa, Enrique,Nagel, Yvonne,Najera, Carmen

, p. 2328 - 2343 (2008/02/08)

Different L-prolinamides 21, prepared from L-proline and chiral β-amino alcohols are active bifunctional catalysts for the direct nitro-Michael addition of ketones to β-nitrostyrenes. In particular, catalyst 21e, prepared from L-proline and (1S,2R?)-cis-1

Novel small organic molecules for a highly enantioselective direct aldol reaction

Tang, Zhuo,Jiang, Fan,Yu, Luo-Ting,Cui, Xin,Gong, Liu-Zhu,Mi, Ai-Qiao,Jiang, Yao-Zhong,Wu, Yun-Dong

, p. 5262 - 5263 (2007/10/03)

Novel organic molecules containing an l-proline amide moiety and a terminal hydroxyl for catalyzing direct asymmetric aldol reactions of aldehydes in neat acetone are designed and prepared. Catalyst 3d, prepared from l-proline and (1S,2S)-diphenyl-2-amino

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