Cas 502765-46-0,2-Oxazolidinone, 3-[(3S)-3-hydroxy-2-[(S)-hydroxyphenylmethyl]-1-oxo-3-phenylpropyl]-4-( phenylmethyl)-, (4S)-

502765-46-0

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Basic information

Product Name: 2-Oxazolidinone, 3-[(3S)-3-hydroxy-2-[(S)-hydroxyphenylmethyl]-1-oxo-3-phenylpropyl]-4-( phenylmethyl)-, (4S)-
Synonyms:
CAS NO:502765-46-0
Molecular Formula: C26H25NO5
Molecular Weight: 431.488
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: 2-Oxazolidinone, 3-[(3S)-3-hydroxy-2-[(S)-hydroxyphenylmethyl]-1-oxo-3-phenylpropyl]-4-( phenylmethyl)-, (4S)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Oxazolidinone, 3-[(3S)-3-hydroxy-2-[(S)-hydroxyphenylmethyl]-1-oxo-3-phenylpropyl]-4-( phenylmethyl)-, (4S)-(502765-46-0)
EPA Substance Registry System: 2-Oxazolidinone, 3-[(3S)-3-hydroxy-2-[(S)-hydroxyphenylmethyl]-1-oxo-3-phenylpropyl]-4-( phenylmethyl)-, (4S)-(502765-46-0)

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: 502765-46-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 502765-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,7,6 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 502765-46:
(8*5)+(7*0)+(6*2)+(5*7)+(4*6)+(3*5)+(2*4)+(1*6)=140
140 % 10 = 0
So 502765-46-0 is a valid CAS Registry Number.

502765-46-0Upstream product

502765-46-0Downstream Products

502765-46-0Relevant academic research and scientific papers

Asymmetric double aldol reaction of chiral acetyloxazolidinone

Furuno, Hiroshi,Inoue, Tadashi,Abiko, Atsushi

, p. 8297 - 8299 (2002)

Treatment of chiral oxazolidinone with Bu2BOTf (2.5 equiv.) and Et3N (3.0 equiv.) quantitatively produced the doubly borylated enolate, which afforded the double aldol products with high diastereoselectivity after reaction with aldehydes.

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