Cas 1126529-55-2,(2S)-N-[(R)-1-(methylsulfonamido)-1-oxo-3-phenylpropan-2-yl]pyrrolidine-2-carboxamide hydrochloride

1126529-55-2

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Basic information

Product Name: (2S)-N-[(R)-1-(methylsulfonamido)-1-oxo-3-phenylpropan-2-yl]pyrrolidine-2-carboxamide hydrochloride
Synonyms:
CAS NO:1126529-55-2
Molecular Formula:
Molecular Weight: 375.876
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: (2S)-N-[(R)-1-(methylsulfonamido)-1-oxo-3-phenylpropan-2-yl]pyrrolidine-2-carboxamide hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: (2S)-N-[(R)-1-(methylsulfonamido)-1-oxo-3-phenylpropan-2-yl]pyrrolidine-2-carboxamide hydrochloride(1126529-55-2)
EPA Substance Registry System: (2S)-N-[(R)-1-(methylsulfonamido)-1-oxo-3-phenylpropan-2-yl]pyrrolidine-2-carboxamide hydrochloride(1126529-55-2)

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: 1126529-55-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1126529-55-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,6,5,2 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1126529-55:
(9*1)+(8*1)+(7*2)+(6*6)+(5*5)+(4*2)+(3*9)+(2*5)+(1*5)=142
142 % 10 = 2
So 1126529-55-2 is a valid CAS Registry Number.

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1126529-55-2Relevant academic research and scientific papers

Sulfonamides of homoproline and dipeptides as organocatalysts for Michael and aldol reactions

Tsandi, Evaggelia,Kokotos, Christoforos G.,Kousidou, Sofia,Ragoussis, Valentine,Kokotos, George

, p. 1444 - 1449 (2009)

Sulfonamides of the non-natural amino acid homoproline and the dipeptide Pro-Phe were synthesised and evaluated for their catalytic activity in Michael and aldol reactions. Sulfonamides of homoproline outperform proline and Pro-Phe in the Michael reaction

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