Cas 1162647-83-7,(S)-2-[3-(di-o-tolylphosphanyl)thiophen-2-yl]-4-isopropyl-4,5-dihydrooxazole

1162647-83-7

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Basic information

Product Name: (S)-2-[3-(di-o-tolylphosphanyl)thiophen-2-yl]-4-isopropyl-4,5-dihydrooxazole
Synonyms: (S)-2-[3-(di-o-tolylphosphanyl)thiophen-2-yl]-4-isopropyl-4,5-dihydrooxazole
CAS NO:1162647-83-7
Molecular Formula:
Molecular Weight: 407.516
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)-2-[3-(di-o-tolylphosphanyl)thiophen-2-yl]-4-isopropyl-4,5-dihydrooxazole(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[3-(di-o-tolylphosphanyl)thiophen-2-yl]-4-isopropyl-4,5-dihydrooxazole(1162647-83-7)
EPA Substance Registry System: (S)-2-[3-(di-o-tolylphosphanyl)thiophen-2-yl]-4-isopropyl-4,5-dihydrooxazole(1162647-83-7)

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: 1162647-83-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1162647-83-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,2,6,4 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1162647-83:
(9*1)+(8*1)+(7*6)+(6*2)+(5*6)+(4*4)+(3*7)+(2*8)+(1*3)=157
157 % 10 = 7
So 1162647-83-7 is a valid CAS Registry Number.

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1162647-83-7Relevant academic research and scientific papers

The synthesis of new HetPHOX ligands and their application to the intermolecular asymmetric heck reaction

Fitzpatrick, Martin O.,Muller-Bunz, Helge,Guiry, Patrick J.

experimental part, p. 1889 - 1895 (2009/09/05)

The synthesis of six members of the HetPHOX ligand class and the application of palladium complexes of these ligands to the intermolecular asymmetric Heck reaction is described, The tert-leucinol-derived ligands proved the most enantioselective, with pall

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