Cas 724772-71-8,(S)-3-((2S,3R)-1-Benzenesulfonyl-2-p-tolyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one

724772-71-8

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Basic information

Product Name: (S)-3-((2S,3R)-1-Benzenesulfonyl-2-p-tolyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one
Synonyms: (S)-3-((2S,3R)-1-Benzenesulfonyl-2-p-tolyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one
CAS NO:724772-71-8
Molecular Formula:
Molecular Weight: 490.58
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)-3-((2S,3R)-1-Benzenesulfonyl-2-p-tolyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-((2S,3R)-1-Benzenesulfonyl-2-p-tolyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one(724772-71-8)
EPA Substance Registry System: (S)-3-((2S,3R)-1-Benzenesulfonyl-2-p-tolyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one(724772-71-8)

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: 724772-71-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 724772-71-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,4,7,7 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 724772-71:
(8*7)+(7*2)+(6*4)+(5*7)+(4*7)+(3*2)+(2*7)+(1*1)=178
178 % 10 = 8
So 724772-71-8 is a valid CAS Registry Number.

724772-71-8Upstream product

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724772-71-8Relevant academic research and scientific papers

Asymmetric halo-Mannich-type reaction provides access to pyrrolidines and β-proline derivatives

Timmons, Cody,Guo, Li,Liu, Junying,Cannon, John F.,Li, Guigen

, p. 7634 - 7639 (2007/10/03)

A new halo-Mannich-type reaction is reported using cyclopropyl carbonyl-derived enolates and sulfonyl-protected imines. Chiral oxazolidinones auxiliaries were found to be effective for completely controlling the stereochemistry of the products. Variations

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