170737-95-8

Basic information

• Product Name: 2-Methoxy-4-chlorophenylacetic acid
• Synonyms: 2-Methoxy-4-chlorophenylacetic acid;(4-Chloro-2-methoxyphenyl)acetic acid;4-Chloro-2-methoxybenzeneacetic acid;4-CHLORO-2-METHOXYPHENYLACETIC ACID（WS203468）;2-(4-chloro-2-methoxyphenyl)acetic acid, 95%
• CAS NO: 170737-95-8
• Molecular Formula: C₉H₉ClO₃
• Molecular Weight: 200.61896
• Mol File: 170737-95-8.mol

Chemical Properties

• Boiling Point: 323.5±27.0 °C(Predicted)
• Appearance: /
• Density: 1.312±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 4.01±0.10(Predicted)
• CAS DataBase Reference: 2-Methoxy-4-chlorophenylacetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methoxy-4-chlorophenylacetic acid(170737-95-8)
• EPA Substance Registry System: 2-Methoxy-4-chlorophenylacetic acid(170737-95-8)

Safety Data

• Hazardous Substances Data: 170737-95-8(Hazardous Substances Data)

Usage

Uses

Used in Biochemical Research:
2-Methoxy-4-chlorophenylacetic acid is used as a critical component in biochemical studies and experimentation. Its reactivity with other molecules is crucial for understanding various biochemical processes and mechanisms.
Used in Molecule Production:
2-Methoxy-4-chlorophenylacetic acid is used as a key ingredient in the synthesis of certain molecules, contributing to the advancement of biochemistry and related fields.
Used in Reaction Catalysts:
2-Methoxy-4-chlorophenylacetic acid is utilized as a catalyst in specific biochemical reactions, facilitating the progress of these reactions and potentially leading to the discovery of new compounds or insights into existing ones.

Upstream product

• 170737-92-5 (4-chloro-2-methoxyphenyl)acetonitrile 

Downstream Products

• 193290-23-2 methyl 2-(4-chloro-2-methoxyphenyl)acetate 

Relevant articles and documents

BENZENE COMPOUND HAVING 2 OR MORE SUBSTITUENTS

A superior LXR modulator is provided. A compound represented by the general formula (I): [wherein R1: -COR9 (wherein R9: alkyl, optionally substituted alkoxy or optionally substituted amino); R2: H, OH, alkoxy, optionally substituted amino, etc.; R3: H, optionally substituted alkyl, cycloalkyl, optionally substituted alkoxy, optionally substituted amino, halogeno, etc.; R4 and R5: H, optionally substituted alkyl, halogeno, etc.; R6 and R7: H, alkyl; R8: -X2R10 [wherein R10: -COR11 (wherein R11 : OH, optionally substituted alkoxy, optionally substituted amino, etc.), -SO2R12 (wherein R12: optionally substituted alkyl, optionally substituted amino, etc.), tetrazol-5-yl, etc.; X2: single bond, optionally substituted alkylene, etc.]; X1: -NH-, -O-, -S-, etc.; Y1: optionally substituted phenyl, optionally substituted 5- to 6-membered aromatic heterocyclyl; Y2: optionally substituted aryl, optionally substituted heterocyclyl, etc.] and the like is provided.

SUBSTITUTED ACIDS FOR THE TREATMENT OF RESPIRATORY DISEASES

The invention relates to substituted acids of formula (I), where T,W,X,Y,Z, R1 and R2 as defined in the claims, as useful pharmaceutical compounds for treating asthma and rhinitis, pharmaceutical compositions containing them, and a processes for their preparation.

BENZENE COMPOUND HAVING 2 OR MORE SUBSTITUENTS

Disclosed is an excellent LXR modulator. Specifically disclosed is a compound represented by the general formula (I) below or the like. (I) [In the formula, R1 represents a -COR9 (wherein R9 represents an alkyl, optionally substituted alkoxy or optionally substituted amino); R2 represents an H, OH, alkoxy, optionally substituted amino or the like; R3 represents an H, optionally substituted alkyl, cycloalkyl, optionally substituted alkoxy, optionally substituted amino, halogeno or the like; R4 and R5 respectively represent an H, optionally substituted alkyl, halogeno or the like; R6 and R7 respectively represent an H or alkyl; R8 represents a -X2R10 [wherein R10 represents a -COR11 (wherein R11 represents an OH, optionally substituted alkoxy, optionally substituted amino or the like), -SO2R12 (wherein R12 represents an optionally substituted alkyl, optionally substituted amino or the like), tetrazole-5-yl or the like; and X2 represents a single bond, optionally substituted alkylene or the like]; X1 represents an -NH-, -O-, -S- or the like; Y1 represents an optionally substituted phenyl or optionally substituted 5-membered or 6-membered aromatic heterocyclyl; and Y2 represents an optionally substituted aryl, substituted heterocyclyl or the like.]

1-H-3-aryl-pyrrolidine-2, 4-dione derivatives as pest-control agents

The present invention relates to new 1-H-3-aryl-pyrrolidine-2,4-dione derivatives of the formula (I) in which A, B, G, X, Y and Z have the meanings given in the description, to processes for their preparation, and to intermediates therefor. The compounds