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<(1S)-endo>-(-)-borneol R(P)-methyl phenyl phosphinate ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136835-32-0

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136835-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136835-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136835-32:
(8*1)+(7*3)+(6*6)+(5*8)+(4*3)+(3*5)+(2*3)+(1*2)=140
140 % 10 = 0
So 136835-32-0 is a valid CAS Registry Number.

136835-32-0Relevant academic research and scientific papers

A useful synthesis of (R,R)-1,2-ethanediylbis[(o-methoxyphenyl)phenylphosphine] the ligand of the enantioselective catalyst [Rh(COD) (DIPAMP)]+ BF4-

Schmidt,Riedl,Griesser,Fitz

, p. 655 - 657 (1991)

1,2-Ethanediylbis[(o-methoxyphenyl)phenylphosphine] the ligand of the enantioselective catalyst [Rh(1,5-COD)(DIPAMP)]+ BF4- is prepared from (1S)-bornyl (R)p-methyl(phenyl)phosphinate, which is diastereoselectively formed.

Dynamic Kinetic Resolution of Phosphinic Acid Derivatives via Nucleophilic Substitution at Phosphorus Center

Strzelecka, Dorota,Baok, Olga,Borowski, Piotr,Stankevi?, Marek

supporting information, p. 4922 - 4932 (2018/12/14)

Reaction of racemic phosphinic acid derivatives with chiral alcohols proceeds with predominant formation of one diastereomer. The highest level of enrichment has been obtained for transesterfication of racemic methyl benzylphenylphosphinate (64% de). The

A generalization of the base effect on the diastereoselective synthesis of sulfinic and phosphinic esters

Fernandez, Inmaculada,Khiar, Noureddine,Roca, Aranzazu,Benabra, Abdelhak,Alcudia, Ana,Espartero, Jose L.,Alcudia, Felipe

, p. 2029 - 2032 (2007/10/03)

Various chiral secondary alcohols have been used to study the dependence of the stereochemical outcome of sulfinate and phosphinate ester synthesis on the nature of the base used to catalyse the reaction. From this study it has been shown that the achiral

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