Cas 139564-35-5,(-)-(3R,7aR)-3-Phenyl-5-oxo-7a-(2-methylpropyl)-2,3,5,6,7,7a-hexahydropyrrolo<2,1-b>oxazole

139564-35-5

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Basic information

Product Name: (-)-(3R,7aR)-3-Phenyl-5-oxo-7a-(2-methylpropyl)-2,3,5,6,7,7a-hexahydropyrrolo<2,1-b>oxazole
Synonyms: (-)-(3R,7aR)-3-Phenyl-5-oxo-7a-(2-methylpropyl)-2,3,5,6,7,7a-hexahydropyrrolo<2,1-b>oxazole
CAS NO:139564-35-5
Molecular Formula:
Molecular Weight: 259.348
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: (-)-(3R,7aR)-3-Phenyl-5-oxo-7a-(2-methylpropyl)-2,3,5,6,7,7a-hexahydropyrrolo<2,1-b>oxazole(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(3R,7aR)-3-Phenyl-5-oxo-7a-(2-methylpropyl)-2,3,5,6,7,7a-hexahydropyrrolo<2,1-b>oxazole(139564-35-5)
EPA Substance Registry System: (-)-(3R,7aR)-3-Phenyl-5-oxo-7a-(2-methylpropyl)-2,3,5,6,7,7a-hexahydropyrrolo<2,1-b>oxazole(139564-35-5)

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: 139564-35-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139564-35-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,5,6 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 139564-35:
(8*1)+(7*3)+(6*9)+(5*5)+(4*6)+(3*4)+(2*3)+(1*5)=155
155 % 10 = 5
So 139564-35-5 is a valid CAS Registry Number.

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139564-35-5Relevant academic research and scientific papers

A Simple Asymmetric Synthesis of 2-Substituted Pyrrolidines and 5-Substituted Pyrrolidinones

Burgess, Laurence E.,Meyers, A. I.

, p. 1656 - 1662 (1992)

An efficient procedure for the preparation of the title compounds in high enantiomeric purity has been realized starting from 3-acylpropionic acids.Stereoselective reduction of chiral bicyclic lactams 2a-h, prepared from the corresponding γ-keto acid and

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