Cas 1103535-93-8,(2S,4S)-4-hydroxy-N-[(S)-1-hydroxy-1,1,3-triphenylpropan-2-yl]pyrrolidine-2-carboxamide

1103535-93-8

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Basic information

Product Name: (2S,4S)-4-hydroxy-N-[(S)-1-hydroxy-1,1,3-triphenylpropan-2-yl]pyrrolidine-2-carboxamide
Synonyms: (2S,4S)-4-hydroxy-N-[(S)-1-hydroxy-1,1,3-triphenylpropan-2-yl]pyrrolidine-2-carboxamide
CAS NO:1103535-93-8
Molecular Formula:
Molecular Weight: 416.52
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,4S)-4-hydroxy-N-[(S)-1-hydroxy-1,1,3-triphenylpropan-2-yl]pyrrolidine-2-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4S)-4-hydroxy-N-[(S)-1-hydroxy-1,1,3-triphenylpropan-2-yl]pyrrolidine-2-carboxamide(1103535-93-8)
EPA Substance Registry System: (2S,4S)-4-hydroxy-N-[(S)-1-hydroxy-1,1,3-triphenylpropan-2-yl]pyrrolidine-2-carboxamide(1103535-93-8)

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: 1103535-93-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1103535-93-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,3,5,3 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1103535-93:
(9*1)+(8*1)+(7*0)+(6*3)+(5*5)+(4*3)+(3*5)+(2*9)+(1*3)=108
108 % 10 = 8
So 1103535-93-8 is a valid CAS Registry Number.

1103535-93-8Upstream product

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1103535-93-8Relevant academic research and scientific papers

Organocatalytic activity of 4-hydroxy-prolinamide alcohol with different noncovalent coordination sites in asymmetric Michael and direct aldol reactions

Okuyama, Yuko,Nakano, Hiroto,Watanabe, Yuki,Makabe, Mika,Takeshita, Mitsuhiro,Uwai, Koji,Kabuto, Chizuko,Kwon, Eunsang

, p. 193 - 197 (2009)

4-Hydroxy-prolinamide alcohol with different noncoordination sites as a molecule showed excellent asymmetric catalytic activity in both the Michael reaction (up to 98% ee) and the direct aldol reaction (up to >99% ee), and the catalyzing reactions with hi

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