26118-57-0

Basic information

• Product Name: (4-PROPOXY-PHENYL)-ACETIC ACID
• Synonyms: (4-PROPOXY-PHENYL)-ACETIC ACID;4-PROPOXY-BENZENEACETIC ACID;BENZENEACETIC ACID, 4-PROPOXY-;OTAVA-BB 7020330586;UKRORGSYN-BB BBV-106012
• CAS NO: 26118-57-0
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.23
• Mol File: 26118-57-0.mol
• Article Data: 5

Chemical Properties

• Melting Point: 82-84 °C
• Boiling Point: 331.6±17.0 °C(Predicted)
• Appearance: /
• Density: 1.116±0.06 g/cm3(Predicted)
• PKA: 4.45±0.10(Predicted)
• CAS DataBase Reference: (4-PROPOXY-PHENYL)-ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (4-PROPOXY-PHENYL)-ACETIC ACID(26118-57-0)
• EPA Substance Registry System: (4-PROPOXY-PHENYL)-ACETIC ACID(26118-57-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 26118-57-0(Hazardous Substances Data)

Usage

Uses

(4-Propoxyphenyl)acetic Acid can be used as p38α inhibitor for lung cancer.

Upstream product

• 29056-04-0 (4-propoxyphenyl)acetic acid methyl ester 
• 5349-18-8 4-methylphenol n-propyl ether 
• 5736-86-7 1-(4-propoxyphenyl)ethanone 
• 17138-28-2 (4-hydroxy-phenyl)-acetic acid ethyl ester 
• 50690-52-3 (4-propoxy-phenyl)-acetonitrile 
• 15560-71-1 ethyl 2-(4-(n-propoxy)phenyl)acetate 

Downstream Products

• 36935-43-0 4-n-Butyl-4'-propoxy-α-chlor-trans-stilben 
• 94686-48-3 4,4'-Dipropyloxy-deoxybenzoin 
• 1276022-78-6 3-(1H-benzo[d]imidazol-6-yl)-4,5-bis(4-propoxyphenyl)oxazolidin-2-one 
• 1331821-89-6 3-(1H-benzo[d]imidazol-6-yl)-5-phenyl-4-(4-propoxyphenyl)oxazolidin-2-one 
• 1276023-00-7 C₂₀H₂₃NO₄ 
• 1276023-01-8 C₂₀H₂₇NO₃ 
• 1276023-02-9 C₂₁H₂₅NO₄ 
• 1276023-03-0 C₂₇H₃₁N₃O₄ 
• 1276023-07-4 C₁₇H₁₇NO₃ 
• 1276023-08-5 C₁₇H₂₁NO₂ 
• 1276023-09-6 C₁₈H₁₉NO₃ 
• 1276023-10-9 C₂₄H₂₅N₃O₃ 
• 50690-34-1 2-(4-propoxyphenyl)acetic acid chloride 
• 127035-75-0 2,6-Dimethyl-4-[(E)-2-(4-propoxy-phenyl)-vinyl]-phenol 

Relevant articles and documents

PROCESS FOR SYNTHESIZING PHENYLACETIC ACID BY CARBONYLATION OF TOLUENE

A production process for substituted phenylacetic acids or ester analogues thereof is disclosed. In this process toluene or toluene substituted with various substituents, an alcohol, an oxidant and carbon monoxide are used as raw materials to obtain compounds comprising structure of phenylacetic acid ester or analogues thereof by catalysis of the complex catalyst formed from transition metal and ligand, and such compounds are hydrolyzed to obtain various substituted phenylacetic acid based compounds. This type of compounds and their derivatives serve as important fine chemicals used widely in the industries of pharmaceuticals, pesticides, perfume and the like.

PIPERAZINE AND PIPERIDINE MGLUR5 POTENTIATORS

Compounds of Formula I or pharmaceutically acceptable salts or solvates thereof, wherein A, B, D, Ar1, Ar2, R2, R3, R4, a, m and n are defined in the specification, methods for the use thereof, processes for making and pharmaceutical compositions containing the same.

The action of chlorine on aqueous solutions of ammonium sulphinates.

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