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2-(4-AMINO-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is a versatile chemical compound belonging to the thiazole family. It is an ethyl ester derivative of 2-(4-amino-phenyl)-thiazole-4-carboxylic acid, characterized by the presence of a thiazole ring, an amino-phenyl group, and a carboxylic acid ester. This unique structure endows it with potential applications in organic synthesis, pharmaceutical research, and the development of new drugs.

730234-73-8

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730234-73-8 Usage

Uses

Used in Pharmaceutical Research:
2-(4-AMINO-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as a building block for the synthesis of more complex molecules in pharmaceutical research. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(4-AMINO-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER serves as a valuable compound for the creation of various chemical entities. Its versatile structure enables the synthesis of a wide range of molecules with different functional groups and properties.
Used in Drug Development:
2-(4-AMINO-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is utilized as a key intermediate in the development of new drugs. Its unique chemical properties and structural features make it a promising candidate for the design and synthesis of innovative pharmaceutical agents with potential therapeutic benefits.
Used in Chemical and Biological Investigations:
In chemical and biological research, 2-(4-AMINO-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is employed as a valuable compound for various investigations. Its unique structure and properties allow researchers to explore its potential applications and interactions with other molecules, contributing to the advancement of scientific knowledge in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 730234-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,0,2,3 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 730234-73:
(8*7)+(7*3)+(6*0)+(5*2)+(4*3)+(3*4)+(2*7)+(1*3)=128
128 % 10 = 8
So 730234-73-8 is a valid CAS Registry Number.

730234-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(4-aminophenyl)-1,3-thiazole-4-carboxylate

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

More Details:730234-73-8 SDS

730234-73-8Relevant academic research and scientific papers

Synthesis and evaluation of potent and selective β3 adrenergic receptor agonists containing heterobiaryl carboxylic acids

Shearer, Barry G.,Chao, Esther Y.,Uehling, David E.,Deaton, David N.,Cowan, Conrad,Sherman, Bryan W.,Milliken, Tula,Faison, Walter,Brown, Kathleen,Adkison, Kimberly K.,Lee, Frank

, p. 4670 - 4677 (2008/02/12)

The design, synthesis, and SAR of a novel series of heterobiaryl phenethanolamine β3 adrenergic receptor agonists are described. The furan analogue 49 was shown to elicit a significant dose-dependent lowering of plasma glucose in a rodent model

AMINO ACIDS

-

Page/Page column 39-40, (2008/06/13)

Compounds of formula (I): Z’ -CO-A-B-NH-Z (I) wherein: Z is H or an amino protecting group; Z’ is OH, a protected or activated hydroxyl group or C1; A is an optionally substituted C5-6 arylene group; and B is an optionally substituted C5-6 arylene group.

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