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(3-CHLORO-4-METHYLSULFANYL-PHENYL)-ACETIC ACID METHYL ESTER, with the molecular formula C10H11ClO2S, is a methyl ester derivative of (3-chloro-4-methylsulfanyl-phenyl)acetic acid. This chemical compound is recognized for its potential biological activities and is currently under investigation for its therapeutic properties, which include anti-inflammatory and analgesic effects. Its unique structure and properties render it a valuable asset in the study of organic molecules' interactions with biological systems and in the development of novel pharmaceuticals.

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  • 436141-65-0 Structure
  • Basic information

    1. Product Name: (3-CHLORO-4-METHYLSULFANYL-PHENYL)-ACETIC ACID METHYL ESTER
    2. Synonyms: (3-CHLORO-4-METHYLSULFANYL-PHENYL)-ACETIC ACID METHYL ESTER;3-CHLORO-4-(METHYLTHIO)-BENZENEACETIC ACID METHYL ESTER;BENZENEACETIC ACID, 3-CHLORO-4-(METHYLTHIO)-, METHYL ESTER
    3. CAS NO:436141-65-0
    4. Molecular Formula: C10H11ClO2S
    5. Molecular Weight: 230.71
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 436141-65-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3-CHLORO-4-METHYLSULFANYL-PHENYL)-ACETIC ACID METHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-CHLORO-4-METHYLSULFANYL-PHENYL)-ACETIC ACID METHYL ESTER(436141-65-0)
    11. EPA Substance Registry System: (3-CHLORO-4-METHYLSULFANYL-PHENYL)-ACETIC ACID METHYL ESTER(436141-65-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 436141-65-0(Hazardous Substances Data)

436141-65-0 Usage

Uses

Used in Pharmaceutical Industry:
(3-CHLORO-4-METHYLSULFANYL-PHENYL)-ACETIC ACID METHYL ESTER is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to serve as a building block in the creation of new drugs with potential therapeutic applications.
Used in Research Applications:
In the field of research, (3-CHLORO-4-METHYLSULFANYL-PHENYL)-ACETIC ACID METHYL ESTER is utilized as a valuable tool for studying the interactions between organic molecules and biological systems. This understanding can lead to the development of new pharmaceuticals and a deeper comprehension of molecular interactions.
Used in Drug Development:
(3-CHLORO-4-METHYLSULFANYL-PHENYL)-ACETIC ACID METHYL ESTER is employed as a key component in the development of new drugs, particularly those with anti-inflammatory and analgesic properties. Its potential therapeutic effects make it a promising candidate for further investigation and application in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 436141-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,1,4 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 436141-65:
(8*4)+(7*3)+(6*6)+(5*1)+(4*4)+(3*1)+(2*6)+(1*5)=130
130 % 10 = 0
So 436141-65-0 is a valid CAS Registry Number.

436141-65-0SDS

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 Methyl [3-chloro-4-(methylsulfanyl)phenyl]acetate

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:436141-65-0 SDS

436141-65-0Relevant articles and documents

5-SUBSTITUTED-PYRAZINE OR PYRIDINE GLUCOKINASE ACTIVATORS

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Page 124, (2010/02/07)

The present invention provides a compound according to formula (I) where the substituent designations are provided in the specification. Pharmaceutical compositions comprising a compound according to formula (I) are also provided, said compounds being glucokinase activators which are useful in the treatment of type II diabetes.

Substituted-cycloalkyl and oxygenated-cycloalkyl glucokinase activators

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Page column 15-16, (2010/11/30)

2,3-Di-substituted N-heteroaromatic propionamides with said substitution at the 2-position being a substituted phenyl group and at the 3-position being a polar ring, said propionamides being glucokinase activators which increase insulin secretion in the treatment of type II diabetes.

Fused heteroaromatic glucokinase activators

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, (2008/06/13)

Glucokinase activating amides are useful for increasing insulin secretion in the treatment of type II diabetes.

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