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19728-76-8

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19728-76-8 Usage

General Description

3-Ethoxycarbonylquinolizidine is a chemical compound with the molecular formula C15H17NO2. It is a quinolizidine alkaloid derivative with a chemical structure that includes an ethoxycarbonyl group. 3-Ethoxycarbonylquinolizidine is a synthetic derivative of quinolizidine and has potential pharmaceutical applications due to its biological activities. Quinolizidine alkaloids are known for their diverse pharmacological properties, including antitumor, anti-inflammatory, and antimicrobial activities. The ethoxycarbonyl group in 3-Ethoxycarbonylquinolizidine makes it a promising candidate for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 19728-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,2 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19728-76:
(7*1)+(6*9)+(5*7)+(4*2)+(3*8)+(2*7)+(1*6)=148
148 % 10 = 8
So 19728-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO2/c1-2-15-12(14)10-6-7-11-5-3-4-8-13(11)9-10/h10-11H,2-9H2,1H3

19728-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Ethoxycarbonylquinolizidine

1.2 Other means of identification

Product number -
Other names cis-octahydro-2h-quinolizine-3-carboxylic acid ethyl ester

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:19728-76-8 SDS

19728-76-8Relevant articles and documents

Azabicyclic indole esters as potent 5-HT4 receptor antagonists

Wyman, Paul A.,Gaster, Laramie M.,King, Frank D.,Sutton, Jonathon M.,Ellis, Elizabeth S.,Wardle, Kay A.,Young, Timothy J.

, p. 255 - 261 (2007/10/03)

The synthesis of a series of azabicyclic indole esters is described and their potency reported as 5-HT4 receptor antagonists. Optimization of the most potent compound (19) by preparing the corresponding oxazino[3,2-a]indole ester afforded 34, which had a pIC50 of 9.5 in the guinea pig distal colon longitudinal muscle myenteric plexus preparation.

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