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(RP)-(L-menthyl)methylphenylphosphine is a chiral organophosphorus compound, characterized by its unique structure and properties. It consists of a phenyl group attached to a phosphorus atom, which is bonded to a methyl group and an L-menthyl group. The L-menthyl group is derived from L-menthol, a naturally occurring terpene alcohol, and imparts a distinct chirality to the molecule. (RP)-(L-menthyl)methylphenylphosphine is of interest in various fields, including asymmetric synthesis, where it can serve as a ligand or a catalyst, and in the development of new materials with specific optical properties. Its chiral nature makes it a potential candidate for applications in the pharmaceutical industry, where the stereochemistry of molecules can significantly influence their biological activity.

65440-73-5

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65440-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65440-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,4 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65440-73:
(7*6)+(6*5)+(5*4)+(4*4)+(3*0)+(2*7)+(1*3)=125
125 % 10 = 5
So 65440-73-5 is a valid CAS Registry Number.

65440-73-5Relevant academic research and scientific papers

Nucleophilic substitution of p-stereogenic chlorophosphines: Mechanism, stereochemistry, and stereoselective conversions of diastereomeric secondary phosphine oxides to tertiary phosphines

Ye, Jing-Jing,Nie, Shao-Zhen,Wang, Ji-Ping,Wen, Jing-Hong,Zhang, Yu,Qiu, Mao-Ran,Zhao, Chang-Qiu

, p. 5384 - 5387 (2017/11/07)

A diastereomeric mixture of secondary phosphine oxide is stereospecifically converted to chlorophosphine salt by treatment with oxalyl chloride, which stereoselectively affords P-inverted or retained tertiary phosphines, depending on the substitution with aliphatic or aromatic Grignard reagents, respectively, in high to 99% yield and 99:1 dr. The repulsion of π- electron on aryl to lone electron pair on phosphorus is proposed for the P-retained substitution.

Crystallization-Induced Asymmetric Transformation of a Tertiary Phosphine

Vedejs, Edwin,Donde, Yariv

, p. 2337 - 2343 (2007/10/03)

An equilibrating diastereomer mixture of the tertiary phosphines 5 and 6 (2.5:1 equilibrium ratio) undergoes crystallization-induced asymmetric transformation upon slow evaporation of solvent from refluxing heptane to give a 20:1 ratio in favor of the more stable crystalline isomer 5. The process can also be carried out at room temperature by using iodine to catalyze the interconversion of 5 and 6 via a pentavalent intermediate 8. However, this variation is more sensitive to the purity of the starting phosphine. Crystalline 5 can be converted to the stable borane complex 3, and reductive cleavage of the fluorenyl group using lithium naphthalenide affords the corresponding lithio derivative 10. Alkylation with iodomethane or benzyl bromide affords 13 or 17, respectively, with retention of phosphorus configuration.

Synthesis of Phosphines Having Chiral Organic Groups Ligated to Chiral Phosphorus

Valentine, Donald,Blount, John F.,Toth, Katherine

, p. 3691 - 3698 (2007/10/02)

Both R and S phosphorus epimers of menthylmethylphenylphosphine and its phoshine oxide and of neomenthylmethylphenylphosphine and its phosphine oxide were prepared.The menthylmethylphenylphosphine oxides were prepared from neomenthyldiphenylphosphine by a

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