Cas 1031790-06-3,(2R)-N-{2-[(S)-4-tert-butyl-4,5-dihydrooxazol-2-yl]phenyl}pyrrolidine-2-carboxamide

1031790-06-3

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Basic information

Product Name: (2R)-N-{2-[(S)-4-tert-butyl-4,5-dihydrooxazol-2-yl]phenyl}pyrrolidine-2-carboxamide
Synonyms: (2R)-N-{2-[(S)-4-tert-butyl-4,5-dihydrooxazol-2-yl]phenyl}pyrrolidine-2-carboxamide
CAS NO:1031790-06-3
Molecular Formula:
Molecular Weight: 315.415
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: (2R)-N-{2-[(S)-4-tert-butyl-4,5-dihydrooxazol-2-yl]phenyl}pyrrolidine-2-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (2R)-N-{2-[(S)-4-tert-butyl-4,5-dihydrooxazol-2-yl]phenyl}pyrrolidine-2-carboxamide(1031790-06-3)
EPA Substance Registry System: (2R)-N-{2-[(S)-4-tert-butyl-4,5-dihydrooxazol-2-yl]phenyl}pyrrolidine-2-carboxamide(1031790-06-3)

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: 1031790-06-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1031790-06-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,1,7,9 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1031790-06:
(9*1)+(8*0)+(7*3)+(6*1)+(5*7)+(4*9)+(3*0)+(2*0)+(1*6)=113
113 % 10 = 3
So 1031790-06-3 is a valid CAS Registry Number.

1031790-06-3Upstream product

955960-57-3 tert-butyl (R)-2-{2-[(S)-4-tert-butyl-4,5-dihydrooxazol-2-yl]phenylcarbamoyl}pyrrolidine-1-carboxylate

1031790-06-3Downstream Products

1031790-06-3Relevant academic research and scientific papers

Oxazoline-substituted prolinamide-based organocatalysts for the direct intermolecular aldol reaction between cyclohexanone and aromatic aldehydes

Doherty, Simon,Knight, Julian G.,McRae, Amy,Harrington, Ross W.,Clegg, William

, p. 1759 - 1766 (2008)

Oxazoline-substituted prolinamides catalyse the direct asymmetric aldol reaction between cyclohexanone and a range of aldehydes to give excellent conversions and enantioselectivities up to 84% under optimum conditions. Reactions were highly substrate-spec

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