Cas 1610880-06-2,(R<sub>P</sub>)-(-)-menthyl[(S)-hydroxy(o-fluorophenyl)methyl]phenylphosphine oxide

1610880-06-2

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Basic information

Product Name: (R_P)-(-)-menthyl[(S)-hydroxy(o-fluorophenyl)methyl]phenylphosphine oxide
Synonyms: (R_P)-(-)-menthyl[(S)-hydroxy(o-fluorophenyl)methyl]phenylphosphine oxide
CAS NO:1610880-06-2
Molecular Formula:
Molecular Weight: 388.462
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (R_P)-(-)-menthyl[(S)-hydroxy(o-fluorophenyl)methyl]phenylphosphine oxide(CAS DataBase Reference)
NIST Chemistry Reference: (R_P)-(-)-menthyl[(S)-hydroxy(o-fluorophenyl)methyl]phenylphosphine oxide(1610880-06-2)
EPA Substance Registry System: (R_P)-(-)-menthyl[(S)-hydroxy(o-fluorophenyl)methyl]phenylphosphine oxide(1610880-06-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1610880-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1610880-06-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,8,8 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1610880-06:
(9*1)+(8*6)+(7*1)+(6*0)+(5*8)+(4*8)+(3*0)+(2*0)+(1*6)=142
142 % 10 = 2
So 1610880-06-2 is a valid CAS Registry Number.

1610880-06-2Upstream product

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1610880-06-2Relevant academic research and scientific papers

Stereogenic phosphorus-induced diastereoselective formation of chiral carbon during nucleophilic addition of chiral H-P species to aldehydes or ketones

Zhang, He,Sun, Yong-Ming,Yao, Lan,Ji, Si-Yu,Zhao, Chang-Qiu,Han, Li-Biao

supporting information, p. 1329 - 1333 (2014/05/06)

P,C-Stereogenic α-hydroxyl phosphinates or phosphine oxides were prepared from the additions of (RP)-phosphinate to ketones or (R P)-phosphine oxide to aldehydes, respectively, catalyzed by bases at room temperature in up to >99:1 di

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