Cas 623158-03-2,(R,R,R,R,R)-ethyl 5-phenyl-4-{[bis(1'-phenyl-ethyl)]carbamoyl}-pyrrolidine-2-carboxylate

623158-03-2

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Basic information

Product Name: (R,R,R,R,R)-ethyl 5-phenyl-4-{[bis(1'-phenyl-ethyl)]carbamoyl}-pyrrolidine-2-carboxylate
Synonyms:
CAS NO:623158-03-2
Molecular Formula:
Molecular Weight: 470.612
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: (R,R,R,R,R)-ethyl 5-phenyl-4-{[bis(1'-phenyl-ethyl)]carbamoyl}-pyrrolidine-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R,R,R,R,R)-ethyl 5-phenyl-4-{[bis(1'-phenyl-ethyl)]carbamoyl}-pyrrolidine-2-carboxylate(623158-03-2)
EPA Substance Registry System: (R,R,R,R,R)-ethyl 5-phenyl-4-{[bis(1'-phenyl-ethyl)]carbamoyl}-pyrrolidine-2-carboxylate(623158-03-2)

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: 623158-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 623158-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,1,5 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 623158-03:
(8*6)+(7*2)+(6*3)+(5*1)+(4*5)+(3*8)+(2*0)+(1*3)=132
132 % 10 = 2
So 623158-03-2 is a valid CAS Registry Number.

623158-03-2Upstream product

623158-03-2Downstream Products

623158-03-2Relevant academic research and scientific papers

Silver acetate catalysed asymmetric 1,3-dipolar cycloadditions of imines and chiral acrylamides

Nyerges, Miklós,Bendell, David,Arany, Andrea,Hibbs, David E.,Coles, Simon J.,Hursthouse, Michael B.,Groundwater, Paul W.,Meth-Cohn, Otto

, p. 947 - 950 (2003)

N-Metallated azomethine ylides 5 were generated by the reaction of arylidene glycine imines 1 with AgOAc and triethylamine. These azomethine ylides undergo cycloaddition to chiral acrylamides 2 with excellent diastereoselectivity. The configuration of two

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