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Ethanone, 1-(4-iodo-2-thienyl)-, also known as 4-iodo-2-thienyl-acetone, is a chemical compound characterized by a ketone group attached to a thienyl ring, with an iodine atom positioned at the fourth position of the ring. This unique structure endows it with versatile reactivity and potential medicinal properties, making it a valuable compound in the realms of organic synthesis and pharmaceutical research.

33148-75-3

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33148-75-3 Usage

Uses

Used in Organic Synthesis:
Ethanone, 1-(4-iodo-2-thienyl)is utilized as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its reactivity allows for the formation of new chemical bonds and the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Ethanone, 1-(4-iodo-2-thienyl)is employed as a starting material for the development of new drugs. Its unique structure and potential medicinal properties make it a promising candidate for the discovery and optimization of novel therapeutic agents. It may exhibit various biological activities, such as anti-inflammatory, antimicrobial, or anticancer properties, which can be harnessed for the treatment of various diseases and conditions.
Used in Drug Discovery and Development:
Ethanone, 1-(4-iodo-2-thienyl)serves as a valuable tool in drug discovery and development due to its potential to modulate biological targets and pathways. Its unique structure allows for the design and synthesis of new drug candidates with improved potency, selectivity, and pharmacokinetic properties. Researchers can use Ethanone, 1-(4-iodo-2-thienyl)- to explore its interactions with various biological targets, leading to the identification of novel therapeutic agents with potential clinical applications.
Used in the Study of Organic Chemistry:
The unique structure and properties of Ethanone, 1-(4-iodo-2-thienyl)make it an intriguing target for further study in the field of organic chemistry. Researchers can investigate its reactivity, stability, and other chemical properties to gain insights into the fundamental principles governing the behavior of similar compounds. This knowledge can be applied to the design and synthesis of new molecules with tailored properties and applications in various fields, including materials science, catalysis, and environmental chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 33148-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,4 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33148-75:
(7*3)+(6*3)+(5*1)+(4*4)+(3*8)+(2*7)+(1*5)=103
103 % 10 = 3
So 33148-75-3 is a valid CAS Registry Number.

33148-75-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Iod-5-acetyl-thiophen

1.2 Other means of identification

Product number -
Other names 1-(4-Iodo-thiophen-2-yl)-ethanone

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:33148-75-3 SDS

33148-75-3Upstream product

33148-75-3Downstream Products

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