Cas 1037077-01-2,(E)-1-[N-benzyl-N-{(1S)-(+)-10-camphorsulfonyl}amino]-2-diphenylthiophosphinyl-1-phenylethene

1037077-01-2

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Basic information

Product Name: (E)-1-[N-benzyl-N-{(1S)-(+)-10-camphorsulfonyl}amino]-2-diphenylthiophosphinyl-1-phenylethene
Synonyms:
CAS NO:1037077-01-2
Molecular Formula:
Molecular Weight: 639.819
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: (E)-1-[N-benzyl-N-{(1S)-(+)-10-camphorsulfonyl}amino]-2-diphenylthiophosphinyl-1-phenylethene(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-[N-benzyl-N-{(1S)-(+)-10-camphorsulfonyl}amino]-2-diphenylthiophosphinyl-1-phenylethene(1037077-01-2)
EPA Substance Registry System: (E)-1-[N-benzyl-N-{(1S)-(+)-10-camphorsulfonyl}amino]-2-diphenylthiophosphinyl-1-phenylethene(1037077-01-2)

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: 1037077-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1037077-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,0,7 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1037077-01:
(9*1)+(8*0)+(7*3)+(6*7)+(5*0)+(4*7)+(3*7)+(2*0)+(1*1)=122
122 % 10 = 2
So 1037077-01-2 is a valid CAS Registry Number.

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1037077-01-2Relevant academic research and scientific papers

Regio- and stereoselective hydroamidation of 1-alkynylphosphine sulfides catalyzed by cesium base

Kondoh, Azusa,Yorimitsu, Hideki,Oshima, Koichiro

supporting information; experimental part, p. 3093 - 3095 (2009/05/27)

(Chemical Equation Presented) Regio- and stereoselective hydroamidation of 1-alkynylphosphine sulfides proceeds in the presence of cesium carbonate to provide (E)-2-amino-1-thiophosphinyl-1-alkenes. Asymmetric hydrogenation of the adducts catalyzed by an

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