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(3-chloro-4-cyanophenyl)acetic acid methyl ester is a methyl ester derivative of (3-chloro-4-cyanophenyl)acetic acid with the molecular formula C10H8ClNO2. It is a white to off-white crystalline solid that is slightly soluble in water and soluble in most organic solvents. (3-chloro-4-cyanophenyl)acetic acid methyl ester is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals and is known for its reactivity and versatility in chemical reactions.

496856-45-2

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496856-45-2 Usage

Uses

Used in Pharmaceutical Industry:
(3-chloro-4-cyanophenyl)acetic acid methyl ester is used as an intermediate in the synthesis of various pharmaceuticals for its reactivity and versatility in chemical reactions.
Used in Agrochemical Industry:
(3-chloro-4-cyanophenyl)acetic acid methyl ester is used as an intermediate in the synthesis of agrochemicals for its reactivity and versatility in chemical reactions.
Used in Organic Synthesis:
(3-chloro-4-cyanophenyl)acetic acid methyl ester is used as a building block in organic synthesis for its reactivity and versatility in chemical reactions.
Used in Scientific Research:
(3-chloro-4-cyanophenyl)acetic acid methyl ester is used as a research chemical for various scientific studies and applications due to its reactivity and versatility in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 496856-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,6,8,5 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 496856-45:
(8*4)+(7*9)+(6*6)+(5*8)+(4*5)+(3*6)+(2*4)+(1*5)=222
222 % 10 = 2
So 496856-45-2 is a valid CAS Registry Number.

496856-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(3-chloro-4-cyanophenyl)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:496856-45-2 SDS

496856-45-2Relevant academic research and scientific papers

ARYL OR N-HETEROARYL SUBSTITUTED METHANESULFONAMIDE DERIVATIVES AS VANILLOID RECEPTOR LIGANDS

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Page/Page column 61, (2013/04/13)

The invention relates to aryl or N-heteroaryl substituted methanesulfonamide derivatives of Formula (I) as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

Aryl or N-heteroaryl Substituted Methanesulfonamide Derivatives as Vanilloid Receptor Ligands

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Paragraph 0477; 0480, (2013/04/10)

The invention relates to aryl or N-heteroaryl substituted methanesulfonamide derivatives as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

Amine Substituted Methanesulfonamide Derivatives as Vanilloid Receptor Ligands

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Paragraph 0525; 0528; 0537, (2013/04/10)

The invention relates to amine substituted methanesulfonamide derivatives as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

AMINE SUBSTITUTED METHANESULFONAMIDE DERIVATIVES AS VANILLOID RECEPTOR LIGANDS

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Page/Page column 64, (2013/04/13)

The invention relates to amine substituted methanesulfonamide derivatives of formula (I) as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

SUBSTITUTED PYRAZOLYL-BASED CARBOXAMIDE AND UREA DERIVATIVES BEARING A PHENYL MOIETY SUBSTITUTED WITH AN N-CONTAINING GROUP AS VANILLOID RECEPTOR LIGANDS

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Page/Page column 69; 70, (2013/05/23)

The invention relates to substituted pyrazolyl-based carboxamide and urea derivatives of formula (R) bearing a phenyl moiety substituted with an N-containing group as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

3,4,5-Trisubstituted isoxazoles as novel PPARδ agonists: Part 1

Epple, Robert,Russo, Ross,Azimioara, Mihai,Cow, Christopher,Xie, Yongping,Wang, Xing,Wityak, John,Karanewsky, Don,Gerken, Andrea,Iskandar, Maya,Saez, Enrique,Martin Seidel,Tian, Shin-Shay

, p. 4376 - 4380 (2007/10/03)

We report the identification of a novel series of trisubstituted isoxazoles as PPAR activators from a high-throughput screen. A series of structural optimizations led to improved efficacy and excellent functional receptor selectivity for PPARδ. The isoxazoles represent a series of agonists which display a scaffold that lies outside the typical PPAR agonist motif.

COMPOUNDS AND COMPOSITIONS AS PPAR MODULATORS

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Page/Page column 27-28, (2010/02/14)

The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of the Peroxisome Proliferator-Activated Receptor (PPAR) families, particularly the activity of PPAR.

COMPOUNDS AND COMPOSITIONS AS PPAR MODULATORS

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Page/Page column 25-26, (2010/02/14)

The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of the Peroxisome Proliferator-Activated Receptor (PPAR) families, particularly the activity of PPAR .

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