Cas 463304-63-4,(4S,3'S)-3-[3-hydroxy-3-(1H-imidazol-4-yl)-3-(2-naphthyl)propanoyl]-4-phenyl-1,3-oxazolidin-2-one

463304-63-4

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Basic information

Product Name: (4S,3'S)-3-[3-hydroxy-3-(1H-imidazol-4-yl)-3-(2-naphthyl)propanoyl]-4-phenyl-1,3-oxazolidin-2-one
Synonyms: (4S,3'S)-3-[3-hydroxy-3-(1H-imidazol-4-yl)-3-(2-naphthyl)propanoyl]-4-phenyl-1,3-oxazolidin-2-one
CAS NO:463304-63-4
Molecular Formula:
Molecular Weight: 427.459
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,3'S)-3-[3-hydroxy-3-(1H-imidazol-4-yl)-3-(2-naphthyl)propanoyl]-4-phenyl-1,3-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S,3'S)-3-[3-hydroxy-3-(1H-imidazol-4-yl)-3-(2-naphthyl)propanoyl]-4-phenyl-1,3-oxazolidin-2-one(463304-63-4)
EPA Substance Registry System: (4S,3'S)-3-[3-hydroxy-3-(1H-imidazol-4-yl)-3-(2-naphthyl)propanoyl]-4-phenyl-1,3-oxazolidin-2-one(463304-63-4)

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: 463304-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 463304-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,3,3,0 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 463304-63:
(8*4)+(7*6)+(6*3)+(5*3)+(4*0)+(3*4)+(2*6)+(1*3)=134
134 % 10 = 4
So 463304-63-4 is a valid CAS Registry Number.

463304-63-4Upstream product

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463304-63-4Relevant academic research and scientific papers

Highly Enantioselective Reformatsky Reaction of Ketones: Chelation-Assisted Enantioface Discrimination

Ojida, Akio,Yamano, Toru,Taya, Naohiro,Tasaka, Akihiro

, p. 3051 - 3054 (2007/10/03)

(Matrix Presented) Highly enantioselective Reformatsky reaction of ketones was accomplished using cinchona alkaloids as chiral ligands. Chelation with the sp2-nitrogen adjacent to the reactive carbonyl center contributed the enantioface discrim

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