Cas 132075-98-0,[(S)-1-((3aS,7aS)-1,3-Dimethyl-2-oxo-octahydro-2λ<sup>5</sup>-benzo[1,3,2]diazaphosphol-2-yl)-2-phenyl-ethyl]-[1,3]dithiolan-2-ylidene-amine

132075-98-0

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Basic information

Product Name: [(S)-1-((3aS,7aS)-1,3-Dimethyl-2-oxo-octahydro-2λ⁵-benzo[1,3,2]diazaphosphol-2-yl)-2-phenyl-ethyl]-[1,3]dithiolan-2-ylidene-amine
Synonyms:
CAS NO:132075-98-0
Molecular Formula:
Molecular Weight: 409.557
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: [(S)-1-((3aS,7aS)-1,3-Dimethyl-2-oxo-octahydro-2λ⁵-benzo[1,3,2]diazaphosphol-2-yl)-2-phenyl-ethyl]-[1,3]dithiolan-2-ylidene-amine(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-1-((3aS,7aS)-1,3-Dimethyl-2-oxo-octahydro-2λ⁵-benzo[1,3,2]diazaphosphol-2-yl)-2-phenyl-ethyl]-[1,3]dithiolan-2-ylidene-amine(132075-98-0)
EPA Substance Registry System: [(S)-1-((3aS,7aS)-1,3-Dimethyl-2-oxo-octahydro-2λ⁵-benzo[1,3,2]diazaphosphol-2-yl)-2-phenyl-ethyl]-[1,3]dithiolan-2-ylidene-amine(132075-98-0)

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: 132075-98-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132075-98-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,7 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132075-98:
(8*1)+(7*3)+(6*2)+(5*0)+(4*7)+(3*5)+(2*9)+(1*8)=110
110 % 10 = 0
So 132075-98-0 is a valid CAS Registry Number.

132075-98-0Upstream product

132075-98-0Downstream Products

66609-42-5 D-Phenylalanine phosphonate

132075-98-0Relevant academic research and scientific papers

A versatile asymmetric synthesis of α-amino α-alkyl-phosphonic acids of high enantiomeric purity

Hanessian, Stephen,Bennani, Youssef L.

, p. 6465 - 6468 (1990)

A general protocol for the synthesis of α-amino-α- alkyl phosphonic acids in either enantiomeric form is described based on the alkylation of chiral bicyclic phosphonamides derived from (R,R)- and (S,S)-1,2-diaminocyclohexane.

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