Cas 1193393-19-9,tert-butyl-(S)-3-methyl-1-oxo-1-(6-((S)-pyrrolidine-2-carboxamido)pyridin-2-ylamino)butan-2-ylcarbamate

1193393-19-9

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Basic information

Product Name: tert-butyl-(S)-3-methyl-1-oxo-1-(6-((S)-pyrrolidine-2-carboxamido)pyridin-2-ylamino)butan-2-ylcarbamate
Synonyms:
CAS NO:1193393-19-9
Molecular Formula:
Molecular Weight: 405.497
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: tert-butyl-(S)-3-methyl-1-oxo-1-(6-((S)-pyrrolidine-2-carboxamido)pyridin-2-ylamino)butan-2-ylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl-(S)-3-methyl-1-oxo-1-(6-((S)-pyrrolidine-2-carboxamido)pyridin-2-ylamino)butan-2-ylcarbamate(1193393-19-9)
EPA Substance Registry System: tert-butyl-(S)-3-methyl-1-oxo-1-(6-((S)-pyrrolidine-2-carboxamido)pyridin-2-ylamino)butan-2-ylcarbamate(1193393-19-9)

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: 1193393-19-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1193393-19-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,3,3,9 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1193393-19:
(9*1)+(8*1)+(7*9)+(6*3)+(5*3)+(4*9)+(3*3)+(2*1)+(1*9)=169
169 % 10 = 9
So 1193393-19-9 is a valid CAS Registry Number.

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1193393-19-9Relevant academic research and scientific papers

Enamine-metal lewis acid bifunctional catalysis: Application to direct asymmetrie aldol reaction of ketones

Xu, Zhenghu,Daka, Philias,Budik, Ilya,Wang, Hong,Bai, Fu-Quan,Zhang, Hong-Xing

supporting information; experimental part, p. 4581 - 4585 (2009/12/06)

Unprecedented bifunctional enamine-metal Lewis acid, catalysts have been developed. In this bifunctional catalytic system, a tridentate ligand tethered with a chiral secondary amine was designed to solve the acid-base self-quenching problem leading to cat

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