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2-Acetyl-4,5-dichlorothiophene is a heterocyclic chemical compound characterized by a thiophene ring with two chlorine atoms at positions 4 and 5, and an acetyl group at position 2. It is widely utilized in the chemical and pharmaceutical industries due to its versatile chemical properties and potential applications in the synthesis of various organic compounds.

57681-59-1

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57681-59-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Acetyl-4,5-dichlorothiophene is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the molecular structures of different drugs. Its unique chemical properties allow it to contribute to the development of new medications with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 2-acetyl-4,5-dichlorothiophene is employed as a building block in the creation of agrochemicals, such as pesticides and herbicides. Its chemical structure can be modified to target specific pests or weeds, enhancing the effectiveness of these products in agricultural settings.
Used in Dye and Pigment Production:
2-Acetyl-4,5-dichlorothiophene is used as a key component in the production of dyes and pigments due to its ability to impart color to various materials. Its presence in these compounds contributes to the vibrancy and stability of the colors in different applications, such as textiles, plastics, and inks.
Used in Fragrance Industry:
2-ACETYL-4,5-DICHLOROTHIOPHENE is also utilized in the fragrance industry as a building block for creating various scent compounds. Its unique chemical structure allows it to contribute to the development of distinct and complex fragrances used in perfumes, cosmetics, and other scented products.
Used in Medicinal Chemistry Research:
2-Acetyl-4,5-dichlorothiophene has been studied for its potential biological and pharmacological activities, making it an important molecule in the field of medicinal chemistry. Its exploration in research settings aims to uncover new therapeutic applications and contribute to the advancement of drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 57681-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,8 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57681-59:
(7*5)+(6*7)+(5*6)+(4*8)+(3*1)+(2*5)+(1*9)=161
161 % 10 = 1
So 57681-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Cl2OS/c1-3(9)5-2-4(7)6(8)10-5/h2H,1H3

57681-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4,5-dichlorothiophen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(4,5-Dichlor-2-thienyl)-ethanon

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:57681-59-1 SDS

57681-59-1Relevant academic research and scientific papers

AMINOPYRIMIDINE COMPOUNDS AND METHODS OF USE

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Page/Page column 33-34, (2010/11/08)

The invention relates to aminopyrimidine compounds useful for treating diseases mediated by polo-like kinase 1 (Plk1). The invention also relates to the therapeutic use of such aminopyrimidine compounds and compositions thereof in treating disease states associated with abnormal cell growth and unwanted cell proliferation.

THIOPHENE ETHANOLAMINES

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, (2008/06/13)

Thiophene ethanolamines substituted on the nitrogen atom with an alkyl or aralkyl radical and optionally substituted on the thiophene portion, are disclosed. The thiophene ethanolamines possess antihypertensive and . beta.-receptor blocking activities. Me

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