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2-(2-CHLORO-ACETYLAMINO)-5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER is a complex organic chemical compound characterized by a cyclopentathiophene ring structure, featuring a carboxylic acid ethyl ester group and a chloroacetylamine moiety. Its unique molecular architecture and functional groups may endow it with specific reactivity and potential biological activity, making it a candidate for various applications in pharmaceuticals, organic synthesis, and organic chemistry research.

203385-15-3

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203385-15-3 Usage

Uses

Used in Pharmaceutical Industry:
2-(2-CHLORO-ACETYLAMINO)-5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER is used as a potential pharmaceutical agent for its possible biological activity, which may be explored for therapeutic applications, including the development of new drugs or drug candidates.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(2-CHLORO-ACETYLAMINO)-5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER serves as a precursor for the synthesis of other complex organic molecules, contributing to the creation of novel chemical entities with potential applications in various industries.
Used in Organic Chemistry Research:
As a research tool in organic chemistry, 2-(2-CHLORO-ACETYLAMINO)-5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER is utilized to study its reactivity, properties, and potential interactions with other molecules, aiding in the advancement of chemical knowledge and the discovery of new reaction pathways or mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 203385-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,3,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 203385-15:
(8*2)+(7*0)+(6*3)+(5*3)+(4*8)+(3*5)+(2*1)+(1*5)=103
103 % 10 = 3
So 203385-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H14ClNO3S/c1-2-17-12(16)10-7-4-3-5-8(7)18-11(10)14-9(15)6-13/h2-6H2,1H3,(H,14,15)

203385-15-3SDS

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-[(2-chloroacetyl)amino]-5,6-dihydro-4H-cyclopenta[b]thiophene-3-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:203385-15-3 SDS

203385-15-3Relevant academic research and scientific papers

Synthesis and analgesic activities of some 2-(benzazolylacetyl)amino-3- ethoxycarbonylthiophene derivatives

Demirayak, Seref,Karaburun, Ahmet C.,Kayagil, Ismail,Ucucu, Umit,Beis, Rana

, p. 1841 - 1848 (2005)

In this study, some 2-[2-(benzazole-2-thioxy)acetylamino]-3- ethoxycarbonylthiophene and 2-[2-(benzazole-1-yl)acetylamino]-3- ethoxycarbonylthiophene compounds were obtained by the reaction of 2-chloroacetylamino-3-ethoxycarbonylthiophene derivatives and a suitable benzazole-2-thione or benzimidazole derivatives. Analgesic activities of the compounds were tested by using tail-flick and tail-immersion methods. It is reported that some of the compounds showed remarkable analgesic activities. Copyright Taylor & Francis Inc.

Substituted chloroacetamides as potential cancer stem cell inhibitors: Synthesis and biological evaluation

Athavale, Maithili,Kharkar, Prashant S.,Padhariya, Komal N.,Srivastava, Sangeeta

, (2019/12/15)

Cancer kills, irrespective of geographical and cultural origin. Novel modalities for treating cancer are desperately needed. Cancer stem cells (CSCs), main culprits behind chemoresistance and tumor relapse, are one of the few logical choices. Herein, we r

2-(3,4-dihydro-4-oxothieno[2,3-d]pyrimidin-2-ylthio) acetamides as a new class of falcipain-2 inhibitors. 3. design, synthesis and biological evaluation

Zhu, Jin,Chen, Tong,Liu, Jie,Ruoqun, Ma.,Lu, Weiqiang,Huang, Jin,Li, Honglin,Li, Jian,Jiang, Hualiang

experimental part, p. 785 - 797 (2009/05/27)

The cysteine protease falcipain-2 (FP-2) of Plasmodium falciparum is a principal cysteine protease and an essential hemoglobinase of erythrocytic P. falciparum trophozoites, making it become an attractive target enzyme for developing anti-malarial drugs.

ANTHELMINTIC AND INSECTICIDAL THIOPHENE DERIVATIVES

-

Page 22-23, (2008/06/13)

Novel anthelmintic compositions containing thiophene derivatives as active ingredients are disclosed.

Synthesis and biological evaluation of new cyclopenteno[b]thiophene derivatives as local anesthetic and antiarrhythmic agents

Al-Obaid,El-Subbagh,Al-Shabanah,Mahran

, p. 24 - 28 (2007/10/03)

A series of ethyl 2-substituted amino-cyclopenteno[b]thiophen-3-carboxylates was synthesized as a carticaine analogues and evaluated for their local anesthetic and antiarrhythmic activity. Compounds ethyl 2-[1-oxo-2-(ethylamino)ethylamino]- (4a), ethyl 2-

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