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N-Acetyl-N-methyl-(R)-phenylalanin-methylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70872-39-8

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70872-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70872-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70872-39:
(7*7)+(6*0)+(5*8)+(4*7)+(3*2)+(2*3)+(1*9)=138
138 % 10 = 8
So 70872-39-8 is a valid CAS Registry Number.

70872-39-8Downstream Products

70872-39-8Relevant academic research and scientific papers

Exploring stereogenic phosphorus: Synthetic strategies for diphosphines containing bulky, highly symmetric substituents

Maienza, Francesca,Spindler, Felix,Thommen, Marc,Pugin, Benoit,Malan, Christophe,Mezzetti, Antonio

, p. 5239 - 5249 (2007/10/03)

Diphosphine ligands bearing highly symmetric, bulky substituents at a stereogenic P atom were prepared, exploiting established protocols, which include the use of chiral synthons such as 3,4- dimethyl-2,5-diphenyl-1,3,2-oxazaphospholidine-2-borane (3a) and phenylmethylchlorophosphine borane (10) and the enantioselective deprotonation of dimethylarylphosphine boranes. However, only (But)(Me)PCH2CH2P(But)Me (8a) could be prepared from 3a. The diphosphines (S,S)-1,2-bis-(mesitylmethylphosphino)ethane, ((S,S)-8b) and (S,S)-1,2- bis(9-anthrylmethylphosphino)ethane ((S,S)-8c), which contain 2,6-disubstituted aryl P-substituents, were prepared by Evans' sparteine-assisted enantioselective deprotonation of P(Ar)(Me)2(BH3) (Ar = mesityl or 9-anthryl), but the enantioselectivity did not exceed 37% ee. The asymmetrically substituted, methylene-bridged diphosphine (2R,4R)-(Ph)(CH3)PCH2P(Mes)(CH3) ((2R,4R)-12) (Mes = mesityl) was prepared by the newly developed stereospecific reaction of the enantiomerically pure chlorophosphine borane PCl(Ph)(Me)(BH3) (10) with the racemic, monolithiated dimethylmesitylphosphine borane P(Mes)(Me)(CH2Li)(BH3). Diastereomerically pure (2R,4R)-12 was obtained with 86% ee. The rhodium(I) derivatives [Rh(COD)(P-P)]BF4 containing the diphosphine ligands 8a, 8b, and 12, as well as the previously reported (S,S)-1,2-bis(1-naphthylphenylphosphino)ethane ((S,S)-8d), were prepared and tested in the enantioselective catalytic hydrogenation of acetamidocinnamates. The best catalytic result (98.6% ee) was obtained with [Rh(COD)(8d)]+ as catalyst and methyl Z-α-acetamidocinnamate as substrate. Some of the catalytic results are discussed in terms of the preferred conformations of the substituents at phosphorus, as calculated by molecular modeling.

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