Cas 144331-19-1,(2S,3S)-2-(1-Benzenesulfonyl-pyrrolidine-2-carbonyloxy)-3-(9-phenyl-9H-fluoren-9-ylamino)-succinic acid dimethyl ester

144331-19-1

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Basic information

Product Name: (2S,3S)-2-(1-Benzenesulfonyl-pyrrolidine-2-carbonyloxy)-3-(9-phenyl-9H-fluoren-9-ylamino)-succinic acid dimethyl ester
Synonyms:
CAS NO:144331-19-1
Molecular Formula:
Molecular Weight: 654.741
EINECS: N/A
Product Categories: N/A
Mol File: 144331-19-1.mol
Article Data: 1

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,3S)-2-(1-Benzenesulfonyl-pyrrolidine-2-carbonyloxy)-3-(9-phenyl-9H-fluoren-9-ylamino)-succinic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-2-(1-Benzenesulfonyl-pyrrolidine-2-carbonyloxy)-3-(9-phenyl-9H-fluoren-9-ylamino)-succinic acid dimethyl ester(144331-19-1)
EPA Substance Registry System: (2S,3S)-2-(1-Benzenesulfonyl-pyrrolidine-2-carbonyloxy)-3-(9-phenyl-9H-fluoren-9-ylamino)-succinic acid dimethyl ester(144331-19-1)

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: 144331-19-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144331-19-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,3,3 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144331-19:
(8*1)+(7*4)+(6*4)+(5*3)+(4*3)+(3*1)+(2*1)+(1*9)=101
101 % 10 = 1
So 144331-19-1 is a valid CAS Registry Number.

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144331-19-1Relevant articles and documents

A stereodivergent chirospecific synthesis of (3R) and (3S) 3-hydroxyaspartates by hydroxylation of aspartate diester enolates

Sardina, F. Javier,Paz, Manuel M.,Fernandez-Megia, Eduardo,De Boer, Richard F.,Alvarez, M. Pilar

, p. 4637 - 4640 (2007/10/02)

A chirospecific and stereodivergent synthesis of N-(9-phenylfluorenyl)-3-hydroxyaspartates by hydroxylation of aspartate enolates is described. The stereochemistry of the newly created chiral center is controlled by the nature of the enolate counterion an

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