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1142209-86-6

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1142209-86-6 Usage

Description

1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid is a chemical compound characterized by the molecular formula C13H16BrNO4S2. It is a derivative of piperidine, featuring a piperidine ring with an attached acetic acid group. 1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid also includes a sulfonyl group and a bromine atom connected to a thienyl ring. The unique chemical structure of 1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid suggests its potential utility in the fields of medicine and pharmaceuticals, given the known biological activities of piperidine derivatives. Further investigation may be necessary to establish its specific characteristics and possible applications.

Uses

Used in Pharmaceutical Applications:
1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid is used as a potential active pharmaceutical ingredient due to its piperidine derivative nature, which is known for exhibiting various biological activities. 1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid's unique structure may allow it to interact with specific biological targets, potentially leading to the development of new medications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid serves as a valuable compound for research purposes. Its structure can be further modified or used as a starting point for the synthesis of new molecules with potential therapeutic applications. This may involve exploring its interactions with various biological receptors, enzymes, or other target molecules to understand its pharmacological profile and optimize its properties for specific medical uses.
Used in Drug Design and Development:
1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid 1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid is utilized in drug design and development as a structural template for creating novel therapeutic agents. Its unique features, such as the sulfonyl group and bromine atom, may provide opportunities for structural modifications that could enhance its pharmacological properties, such as potency, selectivity, and bioavailability. 1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid may also be used in the development of prodrugs, which are biologically inactive compounds that are converted into active drugs within the body.
Used in Chemical Synthesis:
1-[(5-bromo-2-thienyl)sulfonyl]piperidin-4-ylacetic acid can be employed as a synthetic building block or intermediate in the preparation of other complex organic molecules. Its versatile structure allows for various synthetic transformations, which can be exploited to create a diverse range of chemical products with potential applications in different industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1142209-86-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,2,2,0 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1142209-86:
(9*1)+(8*1)+(7*4)+(6*2)+(5*2)+(4*0)+(3*9)+(2*8)+(1*6)=116
116 % 10 = 6
So 1142209-86-6 is a valid CAS Registry Number.

1142209-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name {1-[(5-Bromo-2-thienyl)sulfonyl]piperidin-4-yl}acetic acid

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

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More Details:1142209-86-6 SDS

1142209-86-6Upstream product

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