Cas 1035265-69-0,(R)-1-phenylethanaminium (S)-hydroxy(phenyl)methyl[(S)-hydroxy(phenyl)methyl]phosphinate

1035265-69-0

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Basic information

Product Name: (R)-1-phenylethanaminium (S)-hydroxy(phenyl)methyl[(S)-hydroxy(phenyl)methyl]phosphinate
Synonyms: (R)-1-phenylethanaminium (S)-hydroxy(phenyl)methyl[(S)-hydroxy(phenyl)methyl]phosphinate
CAS NO:1035265-69-0
Molecular Formula:
Molecular Weight: 399.426
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)-1-phenylethanaminium (S)-hydroxy(phenyl)methyl[(S)-hydroxy(phenyl)methyl]phosphinate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-1-phenylethanaminium (S)-hydroxy(phenyl)methyl[(S)-hydroxy(phenyl)methyl]phosphinate(1035265-69-0)
EPA Substance Registry System: (R)-1-phenylethanaminium (S)-hydroxy(phenyl)methyl[(S)-hydroxy(phenyl)methyl]phosphinate(1035265-69-0)

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: 1035265-69-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1035265-69-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,2,6 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1035265-69:
(9*1)+(8*0)+(7*3)+(6*5)+(5*2)+(4*6)+(3*5)+(2*6)+(1*9)=130
130 % 10 = 0
So 1035265-69-0 is a valid CAS Registry Number.

1035265-69-0Upstream product

3886-69-9 (R)-1-phenyl-ethyl-amine

1035265-69-0Downstream Products

1035265-68-9 (-)-(S)-hydroxy(phenyl)methyl[(S)-hydroxy(phenyl)methyl]phosphinic acid

1035265-69-0Relevant academic research and scientific papers

First resolution of (R,R)- and (S,S)-bis(1-hydroxyphenylmethyl)phosphinic acids via diastereomeric salt formation with enantiopure 1-phenylethylamines

Kaboudin, Babak,Haghighat, Hamideh,Yokomatsu, Tsutomu

, p. 862 - 866 (2008)

The resolution of racemic bis(1-hydroxyphenylmethyl)phosphinic acid with enantiopure 1-phenylethylamines via diastereomeric salt formation was investigated. X-ray crystallographic analysis of the salt clearly revealed that (S)-1-phenylethylamine was an ef

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