Cas 107672-34-4,1-[2-(3,4-Dimethoxy-phenyl)-acetyl]-pyrrolidine-2-carboxylic acid ethyl ester

107672-34-4

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Basic information

Product Name: 1-[2-(3,4-Dimethoxy-phenyl)-acetyl]-pyrrolidine-2-carboxylic acid ethyl ester
Synonyms: 1-[2-(3,4-Dimethoxy-phenyl)-acetyl]-pyrrolidine-2-carboxylic acid ethyl ester
CAS NO:107672-34-4
Molecular Formula:
Molecular Weight: 321.373
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: 1-[2-(3,4-Dimethoxy-phenyl)-acetyl]-pyrrolidine-2-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-[2-(3,4-Dimethoxy-phenyl)-acetyl]-pyrrolidine-2-carboxylic acid ethyl ester(107672-34-4)
EPA Substance Registry System: 1-[2-(3,4-Dimethoxy-phenyl)-acetyl]-pyrrolidine-2-carboxylic acid ethyl ester(107672-34-4)

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: 107672-34-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107672-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,7 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107672-34:
(8*1)+(7*0)+(6*7)+(5*6)+(4*7)+(3*2)+(2*3)+(1*4)=124
124 % 10 = 4
So 107672-34-4 is a valid CAS Registry Number.

107672-34-4Upstream product

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107672-35-5 1-[2-(3,4-Dimethoxy-phenyl)-acetyl]-pyrrolidine-2-carboxylic acid

107672-34-4Relevant academic research and scientific papers

A NOVEL AND STEREOSELECTIVE SYNTHESIS OF (+/-)-CEPHALOTAXINE AND ITS ANALOGUE

Yasuda, Shingo,Yamada, Toru,Hanaoka, Miyoji

, p. 2023 - 2026 (1986)

Cephalotaxine (1) and its analogue (3) were stereoselectively synthesized from proline via the pyrrolobenzazepine (4) through Claisen rearrangement, cationic cyclization, and regio- and stereo-selective hydroxylation.

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