26939-01-5

Basic information

• Product Name: (5-chloro-2-methoxyphenyl)acetic acid methyl ester
• Synonyms: (5-chloro-2-methoxyphenyl)acetic acid methyl ester
• CAS NO: 26939-01-5
• Molecular Formula: C₁₀H₁₁ClO₃
• Molecular Weight: 214.64554
• Mol File: 26939-01-5.mol

Chemical Properties

• Boiling Point: 275.2°Cat760mmHg
• Flash Point: 110°C
• Appearance: /
• Density: 1.204g/cm³
• Vapor Pressure: 0.005mmHg at 25°C
• Refractive Index: 1.516
• CAS DataBase Reference: (5-chloro-2-methoxyphenyl)acetic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (5-chloro-2-methoxyphenyl)acetic acid methyl ester(26939-01-5)
• EPA Substance Registry System: (5-chloro-2-methoxyphenyl)acetic acid methyl ester(26939-01-5)

Safety Data

• Hazardous Substances Data: 26939-01-5(Hazardous Substances Data)

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.

InChI:InChI=1/C10H11ClO3/c1-13-9-4-3-8(11)5-7(9)6-10(12)14-2/h3-5H,6H2,1-2H3

Upstream product

• 67-56-1 methanol 
• 7569-63-3 (5-chloro-2-methoxyphenyl)acetyl chloride 
• 124-41-4 sodium methylate 
• 7569-62-2 (5-chloro-2-methoxy-phenyl)-acetic acid 
• 77-78-1 dimethyl sulfate 
• 93-25-4 2-methoxyphenylacetic acid 
• 584-08-7 potassium carbonate 

Downstream Products

• 7569-62-2 (5-chloro-2-methoxy-phenyl)-acetic acid 
• 183720-52-7 methyl 2-(5-chloro-2-methoxyphenyl)-2-(2-nitro-4-(trifluoromethyl)phenyl)acetate 
• 385764-29-4 (+)-3-(5-chloro-2-methoxyphenyl)-1,3-dihydro-6-(trifluoromethyl)-2H-indol-2-one 
• 183720-28-7 3-(5-Chloro-2-methoxyphenyl)-3-fluoro-1,3-dihydro-6-(trifluoromethyl)-2H-indol-2-one 
• 206194-02-7 (S)-(-)-5-Chloro-2-methoxy-α-fluoro-α-[2-nitro-4-(trifluoromethyl)phenyl]benzeneacetic acid 
• 206194-04-9 (R)-(+)-5-Chloro-2-methoxy-α-fluoro-α-[2-nitro-4-(trifluoromethyl)phenyl]benzeneacetic acid 
• 187523-36-0 (-)-BMS-204352 
• 187523-35-9 (S)-(+)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-1,3-dihydro-6-(trifluoromethyl)-2H-indol-2-one 
• 206194-00-5 5-chloro-α-fluoro-2-methoxy-α-[2-nitro-4-(trifluoromethyl)-phenyl]benzeneacetic acid,methyl ester 

Relevant articles and documents

PREPARATION OF 3-FLUORO OXINDOLE DERIVATIVES

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

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

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

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