Cas 240132-23-4,(2SR,4R)-1-benzoyl-2-ethyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester

240132-23-4

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Basic information

Product Name: (2SR,4R)-1-benzoyl-2-ethyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester
Synonyms: (2SR,4R)-1-benzoyl-2-ethyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester
CAS NO:240132-23-4
Molecular Formula:
Molecular Weight: 277.32
EINECS: N/A
Product Categories: N/A
Mol File: 240132-23-4.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: (2SR,4R)-1-benzoyl-2-ethyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2SR,4R)-1-benzoyl-2-ethyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester(240132-23-4)
EPA Substance Registry System: (2SR,4R)-1-benzoyl-2-ethyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester(240132-23-4)

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: 240132-23-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 240132-23-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,1,3 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 240132-23:
(8*2)+(7*4)+(6*0)+(5*1)+(4*3)+(3*2)+(2*2)+(1*3)=74
74 % 10 = 4
So 240132-23-4 is a valid CAS Registry Number.

240132-23-4Upstream product

240132-23-4Downstream Products

240132-24-5 (2SR,4R)-1-benzyl-2-ethyl-4-hydroxy-2-hydroxymethylpyrrolidine

240132-23-4Relevant articles and documents

Ring expansion - Formation of optically active 3-hydroxypiperidines from pyrrolidinemethanol derivatives

Cossy, Janine,Dumas, Cecile,Gomez Pardo, Domingo

, p. 1693 - 1699 (1999)

Treatment of pyrrolidinemethanol derivatives (-)-1, (-)-6, (-)7, 8, (- )-9, (+)-10, (-)-11, and (-)-21 with trifluoroacetic anhydride and then with Et3N afforded, after hydrolysis of the trifluoroacetyl group with NaOH, the optically active -hy

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