Cas 1192134-64-7,(S)-2-{[(2-benzyloxycarbonylaminopropyl)-tert-butoxycarbonylamino]methyl}pyrrolidine-1-carboxylic acid tert-butyl ester

1192134-64-7

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Basic information

Product Name: (S)-2-{[(2-benzyloxycarbonylaminopropyl)-tert-butoxycarbonylamino]methyl}pyrrolidine-1-carboxylic acid tert-butyl ester
Synonyms: (S)-2-{[(2-benzyloxycarbonylaminopropyl)-tert-butoxycarbonylamino]methyl}pyrrolidine-1-carboxylic acid tert-butyl ester
CAS NO:1192134-64-7
Molecular Formula:
Molecular Weight: 491.628
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)-2-{[(2-benzyloxycarbonylaminopropyl)-tert-butoxycarbonylamino]methyl}pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-{[(2-benzyloxycarbonylaminopropyl)-tert-butoxycarbonylamino]methyl}pyrrolidine-1-carboxylic acid tert-butyl ester(1192134-64-7)
EPA Substance Registry System: (S)-2-{[(2-benzyloxycarbonylaminopropyl)-tert-butoxycarbonylamino]methyl}pyrrolidine-1-carboxylic acid tert-butyl ester(1192134-64-7)

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: 1192134-64-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1192134-64-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,1,3 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1192134-64:
(9*1)+(8*1)+(7*9)+(6*2)+(5*1)+(4*3)+(3*4)+(2*6)+(1*4)=137
137 % 10 = 7
So 1192134-64-7 is a valid CAS Registry Number.

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1192134-64-7Relevant academic research and scientific papers

Pyrrolidine-based organocatalysts for enantioselective Michael addition of cyclohexanone to trans-β-nitrostyrene

Carley, Allison P.,Dixon, Sally,Kilburn, Jeremy D.

experimental part, p. 2509 - 2516 (2009/12/08)

A series of readily prepared bifunctional catalysts promote the Michael addition of cyclohexanone to trans-β-nitrostyrene with excellent asymmetric induction. The enantioselection (up to 97%) and diastereoselection (up to 95:5) is comparable to other pyrr

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