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1(2H)-Pyridinecarboxylic acid, 4-[(2,3-dihydro-1H-indol-1-yl)carbonyl]-3,6-dihydro-, ethyl ester is a complex chemical compound that belongs to the class of pyridinecarboxylic acids. It is an ethyl ester derivative of 4-[(2,3-dihydro-1H-indol-1-yl)carbonyl]-3,6-dihydro-1(2H)-pyridinecarboxylic acid. 1(2H)-Pyridinecarboxylic acid,
4-[(2,3-dihydro-1H-indol-1-yl)carbonyl]-3,6-dihydro-, ethyl ester features a pyridine ring, an indole ring, and a carboxylic acid group, which contribute to its diverse chemical and physical properties. Due to its unique structure, it has potential applications in the pharmaceutical industry and may exhibit biological activity and interactions with biological systems.

141474-76-2

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141474-76-2 Usage

Uses

Used in Pharmaceutical Industry:
1(2H)-Pyridinecarboxylic acid, 4-[(2,3-dihydro-1H-indol-1-yl)carbonyl]-3,6-dihydro-, ethyl ester is used as a potential pharmaceutical compound for its possible biological activity and interactions with biological systems. Its unique structure, which includes a pyridine ring, an indole ring, and a carboxylic acid group, may allow it to be utilized in the development of new drugs or therapies.
Used in Chemical Research:
In addition to its potential pharmaceutical applications, 1(2H)-Pyridinecarboxylic acid, 4-[(2,3-dihydro-1H-indol-1-yl)carbonyl]-3,6-dihydro-, ethyl ester can also be used in chemical research. Its diverse chemical and physical properties make it a valuable compound for studying various chemical reactions and processes, potentially leading to new discoveries and advancements in the field of chemistry.
Used in Drug Delivery Systems:
Similar to gallotannin, 1(2H)-Pyridinecarboxylic acid, 4-[(2,3-dihydro-1H-indol-1-yl)carbonyl]-3,6-dihydro-, ethyl ester may be employed in the development of novel drug delivery systems. Its unique structure could be utilized to improve the delivery, bioavailability, and therapeutic outcomes of various drugs, particularly in the context of cancer treatment.
Used in Anticancer Applications:
While specific information on the anticancer properties of 1(2H)-Pyridinecarboxylic acid, 4-[(2,3-dihydro-1H-indol-1-yl)carbonyl]-3,6-dihydro-, ethyl ester is not provided, its potential biological activity and interactions with biological systems suggest that it may be used as an anticancer agent. Further research and development would be necessary to explore its efficacy and potential synergistic effects when combined with conventional chemotherapeutic drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 141474-76-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,4,7 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141474-76:
(8*1)+(7*4)+(6*1)+(5*4)+(4*7)+(3*4)+(2*7)+(1*6)=122
122 % 10 = 2
So 141474-76-2 is a valid CAS Registry Number.

141474-76-2SDS

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 <4-<(2,3-dihydro-1H-indol-1-yl)carbonyl>-1,2,3,6-tetrahydro-1-pyridino>carbamic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 4-(2,3-Dihydro-indole-1-carbonyl)-3,6-dihydro-2H-pyridine-1-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:141474-76-2 SDS

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