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"2H-Pyrrol-2-one, 1,5-dihydro-1-(2-methoxy-1-phenylethyl)-, (R)-" is a complex organic compound belonging to the pyrrolone class. It is characterized by a pyrrolone ring, which is a five-membered ring with one oxygen atom and one nitrogen atom. The compound is a derivative of 1,5-dihydro-2H-pyrrol-2-one, with a 2-methoxy-1-phenylethyl group attached to the nitrogen atom. The "(R)-" notation indicates that the compound has a specific stereochemistry, with the hydroxyl group and the phenyl group on the same side of the double bond in the 2-methoxy-1-phenylethyl moiety. This chiral center gives the compound its unique properties and potential applications in various fields, such as pharmaceuticals and chemical research.

175787-67-4

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175787-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175787-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,7,8 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 175787-67:
(8*1)+(7*7)+(6*5)+(5*7)+(4*8)+(3*7)+(2*6)+(1*7)=194
194 % 10 = 4
So 175787-67-4 is a valid CAS Registry Number.

175787-67-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-((R)-2-Methoxy-1-phenyl-ethyl)-1,5-dihydro-pyrrol-2-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:175787-67-4 SDS

175787-67-4Relevant academic research and scientific papers

Asymmetric routes towards polyfunctionalized pyrrolidines: Synthesis and reactivity of a chiral silyloxypyrrole

Baussanne, Isabelle,Royer, Jacques

, p. 1213 - 1216 (1996)

Starting from O-protected (R)-(-)-phenylglycinol, chiral silyloxypyrrole 5 was prepared in two steps and its reaction with achiral aldehydes under Mukaiyama's reaction conditions was investigated. Addition occurred at the C-5 position of the pyrrolidine ring with complete lk selectivity (except in the case of acetaldehyde) and a moderate to good diastereofacial (RR vs SS) selectivity.

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