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(S)-(+)-methyl(naphthalen-2-yl)(phenyl)phosphane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

381716-99-0

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381716-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 381716-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,1,7,1 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 381716-99:
(8*3)+(7*8)+(6*1)+(5*7)+(4*1)+(3*6)+(2*9)+(1*9)=170
170 % 10 = 0
So 381716-99-0 is a valid CAS Registry Number.

381716-99-0Relevant academic research and scientific papers

About the Inversion Barriers of P-Chirogenic Triaryl-Substituted Phosphanes

Holz, Jens,Jiao, Haijun,Gandelman, Mark,B?rner, Armin

, p. 2984 - 2994 (2018/06/27)

The racemization tendency of acyclic P-chirogenic phosphanes is investigated experimentally and theoretically. Results of these investigations are important for the construction and use of P-chirogenic ligands and organocatalysts frequently used in asymmetric syntheses. Proof is given that triaryl phosphanes undergo easier racemization than compounds in which the phosphorus atom is linked to alkyl substituents. Interestingly, bulky ortho aryl substituents have only a marginal effect, whereas P-naphthyl rings destabilize the compound.

Kinetic resolution of racemic ferrocenylphosphine compounds by enantioselective oxidation using cyclic selenoxides having a chiral ligand

Miyake, Yoshihiro,Yamauchi, Akiyoshi,Nishibayashi, Yoshiaki,Uemura, Sakae

, p. 381 - 387 (2007/10/03)

Cyclic selenoxides having an optically active binaphthyl skeleton work as the reagents for enantioselective oxidation of phosphines to the corresponding phosphine oxides. Treatment of a racemic 2-oxazolin-2-ylferrocenylphosphine with one of the selenoxides in carbon tetrachloride in the presence of phenol affords the corresponding phosphine oxide together with the unreacted starting phosphine, both with moderate enantioselectivities (the phosphine oxide, up to 13% ee; the phosphine, up to 29% ee).

A simple resolution procedure using the Staudinger reaction for the preparation of P-stereogenic phosphine oxides

Andersen,Ramsden,Che,Parvez,Keay

, p. 7478 - 7486 (2007/10/03)

The resolution of a variety of (±)-P-stereogenic phosphines is achieved by exploiting the Staudinger reaction of a (±)-phosphine with enantiopure (1S,2R)-O-(tert-butyldimethylsilyl)isobornyl-10-sulfonyl azide. The resulting mixtures of diastereomeric phosphinimines are generally separable by fractional crystallization or flash chromatography. Subsequent acid-catalyzed hydrolysis provides the corresponding optically pure phosphine oxides in high yields.

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