Cas 154701-62-9,(4S,5S)-4,5-dihydro-2-(2'-bromophenyl)-4-(<(tert-butyl)dimethylsilyloxy>methyl)-5-phenyloxazole

154701-62-9

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Basic information

Product Name: (4S,5S)-4,5-dihydro-2-(2'-bromophenyl)-4-(<(tert-butyl)dimethylsilyloxy>methyl)-5-phenyloxazole
Synonyms: (4S,5S)-4,5-dihydro-2-(2'-bromophenyl)-4-(<(tert-butyl)dimethylsilyloxy>methyl)-5-phenyloxazole
CAS NO:154701-62-9
Molecular Formula:
Molecular Weight: 446.459
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: (4S,5S)-4,5-dihydro-2-(2'-bromophenyl)-4-(<(tert-butyl)dimethylsilyloxy>methyl)-5-phenyloxazole(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5S)-4,5-dihydro-2-(2'-bromophenyl)-4-(<(tert-butyl)dimethylsilyloxy>methyl)-5-phenyloxazole(154701-62-9)
EPA Substance Registry System: (4S,5S)-4,5-dihydro-2-(2'-bromophenyl)-4-(<(tert-butyl)dimethylsilyloxy>methyl)-5-phenyloxazole(154701-62-9)

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: 154701-62-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 154701-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,7,0 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 154701-62:
(8*1)+(7*5)+(6*4)+(5*7)+(4*0)+(3*1)+(2*6)+(1*2)=119
119 % 10 = 9
So 154701-62-9 is a valid CAS Registry Number.

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154701-62-9Relevant academic research and scientific papers

Chiral Mercaptoaryl-oxazolines as Ligands in Enantioselective Copper-Catalyzed 1,4-Additions of Grignard Reagents to Enones

Zhou, Qi-Lin,Pfaltz, Andreas

, p. 4467 - 4478 (2007/10/02)

A series of chiral enantiomerically pure mercaptoaryl-oxazolines has been synthesized.Copper(I) thiolate complexes derived from these ligands proved to be efficient catalysts for the 1,4-addition of Grignard reagents to cyclic enones.Enantioselectivities

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