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3-(4-Chlorophenylthio)butyric acid is a chemical compound with the molecular formula C10H11ClO2S. It is a derivative of butyric acid, containing a 4-chlorophenylthio group attached to the third carbon atom of the butyric acid chain. 3-(4-CHLOROPHENYLTHIO)BUTYRIC ACID has been studied for its potential pharmaceutical and biological activities, including its use as a precursor in the synthesis of drugs and as a potential treatment for certain medical conditions. It has also been investigated for its potential role in modulating the immune system and as an anti-inflammatory agent. Additionally, 3-(4-chlorophenylthio)butyric acid has been studied for its potential effects on lipid metabolism and its potential as a treatment for metabolic disorders.

90919-34-9

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90919-34-9 Usage

Uses

Used in Pharmaceutical Industry:
3-(4-Chlorophenylthio)butyric acid is used as a precursor in the synthesis of drugs for its potential pharmaceutical and biological activities.
Used in Medical Applications:
3-(4-Chlorophenylthio)butyric acid is used as a potential treatment for certain medical conditions due to its potential role in modulating the immune system and as an anti-inflammatory agent.
Used in Immune System Modulation:
3-(4-Chlorophenylthio)butyric acid is used to modulate the immune system, which can be beneficial in treating various immune-related disorders.
Used in Anti-Inflammatory Treatments:
3-(4-Chlorophenylthio)butyric acid is used as an anti-inflammatory agent, which can help in reducing inflammation and associated symptoms in various conditions.
Used in Metabolic Disorders Treatment:
3-(4-Chlorophenylthio)butyric acid is used as a potential treatment for metabolic disorders due to its potential effects on lipid metabolism.

Check Digit Verification of cas no

The CAS Registry Mumber 90919-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,1 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90919-34:
(7*9)+(6*0)+(5*9)+(4*1)+(3*9)+(2*3)+(1*4)=149
149 % 10 = 9
So 90919-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2S/c1-7(6-10(12)13)14-9-4-2-8(11)3-5-9/h2-5,7H,6H2,1H3,(H,12,13)

90919-34-9SDS

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 3-(4-chlorophenyl)sulfanylbutanoic acid

1.2 Other means of identification

Product number -
Other names 3-(4-chlorophenylthio)butyric acid

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:90919-34-9 SDS

90919-34-9Relevant academic research and scientific papers

A structure-taste study of arylsulfonyl(cyclo)alkanecarboxylic acids

Lysiak, Violetta,Ratajczak, Aleksander,Mencel, Agnieszka,Jarzembek, Krystyna,Polanski, Jaroslaw

, p. 671 - 675 (2007/10/03)

A number of sweeteners contain a sulfonyl group. In our current search for new glucophores several new compounds containing such group were obtained. A series of novel 1-phenylsulfonylcyklohexanecarboxylic acids and 2-arylsulfonylalkanecarboxylic acids was obtained and evaluated for their sweet taste quality. It has been found that methyl substituents are of the key importance for the activity of these compounds.

Direct aromatic tert-butylation during the synthesis of thiochroman-4-ones

Clayton, Stephen E.,Gabbutt, Christopher D.,Hepworth, John D.,Mark Heron

, p. 939 - 946 (2007/10/02)

The synthesis of thiochroman-4-ones from thiophenols and 3-methylbut-2-enoic acid effected by methane sulphonic acid is accompanied by tert-butylation of the aromatic ring. 3-Arylthiobutanoic acids, available using β-butyrolactone, are efficiently cyclised in the same manner.

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