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[5-(3,4-dichlorophenyl)-2,3-dihydro-1H-pyrrolizine-6,7-diyl]dimethanediyl bis(benzylcarbamate) is a complex organic compound with a dihydropyrrolizine core, which is linked to two benzylcarbamate groups through dimethanediyl moieties. The presence of the dichlorophenyl group and the dihydropyrrolizine structure indicates potential biological activities, which may be related to neuroreceptor modulation or enzyme inhibition. Its intricate molecular architecture and possible biological functions make it a promising candidate for further research in medicinal chemistry and drug discovery.

74296-46-1

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74296-46-1 Usage

Uses

Used in Pharmaceutical Applications:
[5-(3,4-dichlorophenyl)-2,3-dihydro-1H-pyrrolizine-6,7-diyl]dimethanediyl bis(benzylcarbamate) is used as a potential pharmaceutical agent for its possible neuroreceptor modulation or enzyme inhibition properties. [5-(3,4-dichlorophenyl)-2,3-dihydro-1H-pyrrolizine-6,7-diyl]dimethanediyl bis(benzylcarbamate)'s complex structure and potential biological activities make it an interesting target for the development of new drugs, particularly in the areas of neurological disorders and enzyme-related diseases.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, [5-(3,4-dichlorophenyl)-2,3-dihydro-1H-pyrrolizine-6,7-diyl]dimethanediyl bis(benzylcarbamate) serves as a subject of study for understanding its structure-activity relationships and exploring its potential as a lead compound in drug discovery. [5-(3,4-dichlorophenyl)-2,3-dihydro-1H-pyrrolizine-6,7-diyl]dimethanediyl bis(benzylcarbamate)'s unique features may provide insights into the design of novel therapeutic agents with improved efficacy and selectivity.
Used in Drug Discovery:
[5-(3,4-dichlorophenyl)-2,3-dihydro-1H-pyrrolizine-6,7-diyl]dimethanediyl bis(benzylcarbamate) is utilized as a starting point in drug discovery efforts, where its structure can be optimized and modified to enhance its biological activities and pharmacological properties. [5-(3,4-dichlorophenyl)-2,3-dihydro-1H-pyrrolizine-6,7-diyl]dimethanediyl bis(benzylcarbamate)'s potential as a modulator of neuroreceptors or an inhibitor of specific enzymes makes it a valuable asset in the search for new therapeutic agents to treat various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 74296-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,9 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74296-46:
(7*7)+(6*4)+(5*2)+(4*9)+(3*6)+(2*4)+(1*6)=151
151 % 10 = 1
So 74296-46-1 is a valid CAS Registry Number.

74296-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(benzylcarbamoyloxymethyl)-3-(3,4-dichlorophenyl)-6,7-dihydro-5H-pyrrolizin-1-yl]methyl N-benzylcarbamate

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

1.5 Emergency phone number

Emergency phone number -
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More Details:74296-46-1 SDS

74296-46-1Downstream Products

74296-46-1Relevant academic research and scientific papers

Vinylogous carbinolamine tumor inhibitors. 7. Tumor inhibitory agents: bis-(N-alkylcarbamate) derivatives of 2,3-dihydro-5-(3',4'-dichlorophenyl)-6,7-bis(hydroxymethyl)-1H-pyrrolizine

Anderson,New,Corey

, p. 765 - 767 (2007/10/02)

A series of bis-(N-alkylcarbamate) derivatives of 2,3-dihydro-5-(3',4'-dichlorophenyl)-6,7-bis(hydroxymethyl-1H-pyrrolizine were prepared and evaluated for tumor inhibitory activity (in vivo P388 leukemia).

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