Cas 141964-57-0,(S)-((S)-3-Methylene-2-oxo-5-phenyl-pyrrolidin-1-yl)-phenyl-acetic acid methyl ester

141964-57-0

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Basic information

Product Name: (S)-((S)-3-Methylene-2-oxo-5-phenyl-pyrrolidin-1-yl)-phenyl-acetic acid methyl ester
Synonyms:
CAS NO:141964-57-0
Molecular Formula:
Molecular Weight: 321.376
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: (S)-((S)-3-Methylene-2-oxo-5-phenyl-pyrrolidin-1-yl)-phenyl-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-((S)-3-Methylene-2-oxo-5-phenyl-pyrrolidin-1-yl)-phenyl-acetic acid methyl ester(141964-57-0)
EPA Substance Registry System: (S)-((S)-3-Methylene-2-oxo-5-phenyl-pyrrolidin-1-yl)-phenyl-acetic acid methyl ester(141964-57-0)

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: 141964-57-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141964-57-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,6 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141964-57:
(8*1)+(7*4)+(6*1)+(5*9)+(4*6)+(3*4)+(2*5)+(1*7)=140
140 % 10 = 0
So 141964-57-0 is a valid CAS Registry Number.

141964-57-0Upstream product

142035-32-3 methyl (E)-2-(benzylideneamino)-2-phenylacetate

141964-57-0Downstream Products

141964-57-0Relevant academic research and scientific papers

STEREOCONTROLLED ADDITION OF ORGANOZINC REAGENTS DERIVED FROM 2-(BROMOMETHYLACRYLATES TO CHIRAL IMINES

Dembele, Yenimegue A.,Belaud, Chantal,Hitchcock, Peter,Villieras, Jean

, p. 351 - 354 (1992)

Stereocontrolled addition of isolated organozinc reagents derived from 2-(bromomethyl)acrylates to imines can be achieved with ee ca. 100percent using α-amino esters as chiral auxiliaries.High yields of pure RR or SS N-substituted α-methylene γ-lactams ca

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