Cas 174787-87-2,2-(2-Hydroxy-1-methoxycarbonyl-propyl)-5-(2-oxo-2-phenyl-ethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

174787-87-2

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Basic information

Product Name: 2-(2-Hydroxy-1-methoxycarbonyl-propyl)-5-(2-oxo-2-phenyl-ethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester
Synonyms: 2-(2-Hydroxy-1-methoxycarbonyl-propyl)-5-(2-oxo-2-phenyl-ethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS NO:174787-87-2
Molecular Formula:
Molecular Weight: 405.491
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: 2-(2-Hydroxy-1-methoxycarbonyl-propyl)-5-(2-oxo-2-phenyl-ethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-Hydroxy-1-methoxycarbonyl-propyl)-5-(2-oxo-2-phenyl-ethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester(174787-87-2)
EPA Substance Registry System: 2-(2-Hydroxy-1-methoxycarbonyl-propyl)-5-(2-oxo-2-phenyl-ethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester(174787-87-2)

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: 174787-87-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 174787-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,7,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 174787-87:
(8*1)+(7*7)+(6*4)+(5*7)+(4*8)+(3*7)+(2*8)+(1*7)=192
192 % 10 = 2
So 174787-87-2 is a valid CAS Registry Number.

174787-87-2Upstream product

174787-87-2Downstream Products

174787-87-2Relevant academic research and scientific papers

Studies towards the synthesis of guanidine alkaloids; synthesis of a tricyclic guanidine from succinimide

Louwrier, Saskia,Ostendorf, Martin,Tuynman, Antonin,Hiemstra, Henk

, p. 905 - 908 (1996)

The synthesis of a tricyclic guanidine as a model compound for ptilomycalin A and related guanidine alkaloids is described. The synthesis starts from succinimide and features an N-acyliminium ion coupling, an Eschenmoser sulfide-contraction and an N-guany

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