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(5-chloro-2-methoxyphenyl)acetic acid methyl ester is a colorless, liquid chemical compound derived from the esterification of (5-chloro-2-methoxyphenyl)acetic acid with methanol. It possesses a molecular formula of C10H11ClO3 and exhibits various potential applications in organic synthesis, pharmaceutical chemistry, agrochemicals, and specialty chemicals.

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  • 26939-01-5 Structure
  • Basic information

    1. Product Name: (5-chloro-2-methoxyphenyl)acetic acid methyl ester
    2. Synonyms: (5-chloro-2-methoxyphenyl)acetic acid methyl ester
    3. CAS NO:26939-01-5
    4. Molecular Formula: C10H11ClO3
    5. Molecular Weight: 214.64554
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26939-01-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 275.2°Cat760mmHg
    3. Flash Point: 110°C
    4. Appearance: /
    5. Density: 1.204g/cm3
    6. Vapor Pressure: 0.005mmHg at 25°C
    7. Refractive Index: 1.516
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (5-chloro-2-methoxyphenyl)acetic acid methyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: (5-chloro-2-methoxyphenyl)acetic acid methyl ester(26939-01-5)
    12. EPA Substance Registry System: (5-chloro-2-methoxyphenyl)acetic acid methyl ester(26939-01-5)
  • 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: 26939-01-5(Hazardous Substances Data)

26939-01-5 Usage

Uses

Used in Organic Synthesis:
(5-chloro-2-methoxyphenyl)acetic acid methyl ester is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Chemistry:
In the pharmaceutical industry, (5-chloro-2-methoxyphenyl)acetic acid methyl ester serves as a precursor in drug development. Its functional groups and structural features can be utilized to design and synthesize new pharmaceutical agents with potential therapeutic applications.
Used in Agrochemical Production:
(5-chloro-2-methoxyphenyl)acetic acid methyl ester may have potential use as an intermediate in the production of agrochemicals. Its chemical properties can be harnessed to develop new agrochemicals for crop protection and enhancement of agricultural productivity.
Used in Specialty Chemicals:
(5-chloro-2-methoxyphenyl)acetic acid methyl ester also finds application in the production of specialty chemicals, where its unique characteristics can be exploited to create high-value products for various industries, such as coatings, adhesives, and polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 26939-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,3 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26939-01:
(7*2)+(6*6)+(5*9)+(4*3)+(3*9)+(2*0)+(1*1)=135
135 % 10 = 5
So 26939-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO3/c1-13-9-4-3-8(11)5-7(9)6-10(12)14-2/h3-5H,6H2,1-2H3

26939-01-5SDS

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-(5-chloro-2-methoxyphenyl)acetate

1.2 Other means of identification

Product number -
Other names Benzeneacetic acid,5-chloro-2-methoxy-,methyl ester

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:26939-01-5 SDS

26939-01-5Relevant articles and documents

PREPARATION OF 3-FLUORO OXINDOLE DERIVATIVES

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Page/Page column 10, (2010/02/11)

The present invention relates to novel itermediates of formula (1) wherein the wavy bond ( SIMILAR SIMILAR ) represents the racemate, the (R)-enantiomer or the (S)-enantiomer; and R is hydrogen, a carboxyl-protecting group or a cation of an addition salt;

2- and 2,5-substituted phenylketoenols

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Page column 81, (2010/01/31)

The invention relates to novel phenyl-substituted cyclic ketoenols of the formula (I) in which Het represents one of the groups ?in which A, B, D, G, X and Z are each as defined in the description, to a plurality of processes and intermediates for their preparation, and to their use as pesticides.

The synthesis and characterization of BMS-204352 (MaxiPost) and related 3-fluorooxindoles as openers of maxi-K potassium channels

Hewawasam, Piyasena,Gribkoff, Valentin K.,Pendri, Yadagiri,Dworetzky, Steven I.,Meanwell, Nicholas A.,Martinez, Eduardo,Boissard, Christopher G.,Post-Munson, Debra J.,Trojnacki, Joanne T.,Yeleswaram, Krishnaswamy,Pajor, Lorraine M.,Knipe, Jay,Gao, Qi,Perrone, Robert,Starrett Jr., John E.

, p. 1023 - 1026 (2007/10/03)

3-Aryl-3-fluorooxindoles can be efficiently synthesized in two steps by the addition of an aryl Grignard to an isatin, followed by treatment with DAST. Oxindole 1 (BMS-204352; MaxiPost) can be isolated using chiral HPLC or prepared by employing chiral res

Preparation of 3-fluoro oxindole derivatives

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, (2008/06/13)

The present invention relates to novel intermediates of the formula STR1 wherein the wavy bond () represents the racemate, the (R)-enantiomer or the (S)-enantiomer; and R is hydrogen, a carboxyl-protecting group or a cation of an addition salt; or solvate

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