30044-91-8

Basic information

• Product Name: 3-(4-ETHOXY-3-METHOXYPHENYL)PROPIONIC ACID
• Synonyms: 3-(4-ETHOXY-3-METHOXYPHENYL)PROPIONIC ACID;AKOS BC-2704;3-(4-Ethoxy-3-methoxyphenyl)propanoic acid;(4-ethoxy-3-methoxyphenyl)propanoic acid
• CAS NO: 30044-91-8
• Molecular Formula: C₁₂H₁₆O₄
• Molecular Weight: 224.25304
• Mol File: 30044-91-8.mol

Chemical Properties

• Melting Point: 130～132℃
• Boiling Point: 357.257 °C at 760 mmHg
• Flash Point: 134.126 °C
• Appearance: /
• Density: 1.133 g/cm³
• CAS DataBase Reference: 3-(4-ETHOXY-3-METHOXYPHENYL)PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-ETHOXY-3-METHOXYPHENYL)PROPIONIC ACID(30044-91-8)
• EPA Substance Registry System: 3-(4-ETHOXY-3-METHOXYPHENYL)PROPIONIC ACID(30044-91-8)

Safety Data

• Statements: 36
• Safety Statements: 26
• HazardClass: IRRITANT
• Hazardous Substances Data: 30044-91-8(Hazardous Substances Data)

Usage

Uses

Used in Scientific Research:
3-(4-Ethoxy-3-methoxyphenyl)propionic acid is used as a research chemical for [application reason], contributing to the advancement of scientific knowledge and understanding of its properties and potential applications.
Used in Chemical Synthesis:
3-(4-Ethoxy-3-methoxyphenyl)propionic acid is used as an intermediate in the synthesis of more complex molecules for [application reason], such as pharmaceuticals or other specialty chemicals, where its unique structure and functional groups play a crucial role in the final product's properties and performance.
Used in Analytical Chemistry:
3-(4-Ethoxy-3-methoxyphenyl)propionic acid is used as a reference compound or standard in analytical chemistry for [application reason], such as in the development and validation of analytical methods, quality control, or the identification and quantification of related compounds in various samples.

Upstream product

• 10240-21-8 methyl 4-ethoxy-3-methoxycinnamate 
• 2309-07-1 Methyl ferulate 
• 58168-81-3 4-ethoxy-3-methoxycinnamic acid 

Downstream Products

• 36377-59-0 2-(4-ethoxy-3-methoxyphenyl)ethylamine 
• 858783-47-8 3-(4-ethoxy-3-methoxy-phenyl)-propionic acid amide 

Relevant articles and documents

AMIDES AND METHOD FOR PLANT DISEASE CONTROL WITH THE SAME

N-(α-cyanobenzyl)amide compounds represented by the formula (1): wherein R1 represents a hydrogen atom; a halogen atom; a C1-C6 alkyl group optionally substituted with a halogen atom or the like; or the like, R2 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group or the like, R3 represents a hydrogen atom or the like, R4 represents a C1-C4 alkyl group, a C3-C4 alkenyl group or the like, R5 represents a C1-C4 alkyl group, a C3-C4 alkenyl group, or the like, R6 represents a hydrogen atom or the like, R7 represents a hydrogen atom or the like, R8 represents a hydrogen atom or the like, R9 represents a hydrogen atom or the like, R10 represents a hydrogen atom or the like, R11 represents a hydrogen atom or the like, and R12 represents a hydrogen atom or the like, have excellent control activities against plant diseases.

OLEFIN SATURATION AND ACID REDUCTION OF 3,4-DIMETHOXYCINNAMIC ACID AND DERIVATIVES BY PHANEROCHAETE CHRYSOSPORIUM

The white rot fungus Phanerochaete chrysosporium metabolized 3,4-dimethoxycinnamic acid in shaking and nitrogen sufficient cultures.Metabolites identified included 3-(3,4-dimethoxyphenyl)propionic acid, dimethoxycinnamyl alcohol and 3-(3,4-dimethoxyphenyl)-1-propanol.Significantly smaller amounts of veratryl and vanillyl alcohol were also present.The abundance of the propionic acid and the propanol as metabolic products indicate that olefin saturation and acid reduction are important reactions catalysed under these conditions.Metabolites identified from the metabolism of 3-(3,4-dimethoxyphenyl)-propionic acid included the above 1-propanol as well as veratryl and vanillyl alcohol; the identification of these benzyl alcohol derivatives as metabolites suggests that α,β-bond cleavage of this substrate was preceded by alkane hydroxylation at the α-position.Key Word Index-Phanerochaete chrysosporium; basidiomycete; dimethoxycinnamic acid; ferulic acid; veratryl alcohol; acid reduction; olefin saturation; metabolism