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"2-[2-(4-nitrophenyl)-2-oxoethyl] 1-phenyl pyrrolidine-1,2-dicarboxylate" is a complex organic compound with the molecular formula C23H20N2O7. It is characterized by a pyrrolidine ring, which is a five-membered ring containing one nitrogen atom, and two carboxylate groups attached to the 1 and 2 positions of the pyrrolidine. The compound also features a phenyl group attached to the nitrogen atom and a 4-nitrophenyl group connected to a 2-oxoethyl moiety, which is further linked to the pyrrolidine ring. This structure contributes to its potential applications in pharmaceuticals and chemical research, particularly in the development of compounds with specific biological activities. The compound's synthesis and properties are of interest to chemists due to its intricate structure and the possibility of its derivatives exhibiting useful pharmacological effects.

5915-93-5

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5915-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5915-93-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,1 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5915-93:
(6*5)+(5*9)+(4*1)+(3*5)+(2*9)+(1*3)=115
115 % 10 = 5
So 5915-93-5 is a valid CAS Registry Number.

5915-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-O-[2-(4-nitrophenyl)-2-oxoethyl] 1-O-phenyl pyrrolidine-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2-[2-(4-nitrophenyl)-2-oxoethyl] 1-phenyl (2S)-pyrrolidine-1,2-dicarboxylate

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5915-93-5 SDS

5915-93-5Downstream Products

5915-93-5Relevant academic research and scientific papers

Regiochemistry in aryl radical cyclization onto methylenecycloalkanes

Ishibashi,Kobayashi,Nakashima,Tamura

, p. 9022 - 9027 (2007/10/03)

Bu3SnH-mediated aryl radical cyclization onto methylenecycloalkanes having a phenylthio, an ester, or a nitrile group at the terminus of the alkenic bond provides exclusively exo cyclization products. The results are in sharp contrast to those reported for nonsubstituted methylenecycloalkanes, which give exclusively endo cyclization products. Formation of endo cyclization products has been suggested to be a result of a consecutive 5-exo cyclization of an aryl radical and neophyl rearrangement. The exo-selective aryl radical cyclization offers a new method for synthesizing fused aromatic compounds containing a benzylic quaternary carbon atom.

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