Description

Ethyl 4-hydroxyhydrocinnamate (CAS No. 23795-02-0) is a high-purity organic compound with the molecular formula C₁₁H₁₄O₃, widely utilized in pharmaceutical, cosmetic, and biochemical research. This ester derivative of 4-hydroxyhydrocinnamic acid exhibits excellent stability and solubility in common organic solvents, making it ideal for synthetic applications. Its IUPAC name, ethyl 3-(4-hydroxyphenyl)propanoate, reflects its structural composition, featuring a hydroxyphenyl group attached to a propanoate ester. Suitable for HPLC, GC-MS, and NMR analysis, this compound is rigorously tested to ensure ≥95% purity, meeting the stringent requirements of researchers and industrial scientists. Packaged under inert conditions to prevent degradation, it is available in quantities ranging from grams to kilograms.

Properties

• CAS Number: 23795-02-0
• Complexity: 171
• IUPAC Name: ethyl 3-(4-hydroxyphenyl)propanoate
• InChI: InChI=1S/C11H14O3/c1-2-14-11(13)8-5-9-3-6-10(12)7-4-9/h3-4,6-7,12H,2,5,8H2,1H3
• InChI Key: UFMFPPAZUJDUMY-UHFFFAOYSA-N
• Exact Mass: 194.094294304
• Molecular Formula: C11H14O3
• Molecular Weight: 194.23
• SMILES: CCOC(=O)CCC1=CC=C(C=C1)O
• Topological: 46.5
• Monoisotopic Mass: 194.094294304
• Synonyms: ETHYL 4-HYDROXYHYDROCINNAMATE, 653-330-8, Ethyl 3-(4-hydroxyphenyl)propanoate, 23795-02-0, Ethyl p-hydroxyhydrocinnamate, Ethyl phloretate, Benzenepropanoic acid, 4-hydroxy-, ethyl ester, ethyl 3-(4-hydroxyphenyl)propionate, MFCD00020209, 3-(4-Hydroxyphenyl)propionic acid ethyl ester, Ethyl4-Hydroxyhydrocinnamate, Ethyl3-(4-Hydroxyphenyl)propanoate, SCHEMBL304455, 8R568DFF4T, ethyl 4-hydroxybenzenepropanoate, SCHEMBL5543917, SCHEMBL11750979, DTXSID80371361, UFMFPPAZUJDUMY-UHFFFAOYSA-N, ethyl 4-hydroxyphenyl-3-propanoate, SBB091746, ethyl 3-(4-hydroxyphenyl)-propionate, 4-(3-Ethoxy-3-oxoprop-1-yl)phenol, AKOS006229237, PS-6027, SY018459, DB-026580, 3-(4 Hydroxy-phenyl)-propionic acid ethyl ester, 3-(4-hydroxy-phenyl)-propionic acid ethyl ester

Application

Ethyl 4-hydroxyhydrocinnamate serves as a key intermediate in the synthesis of pharmaceutical agents, particularly those targeting antioxidant and anti-inflammatory pathways. It is also employed in cosmetic formulations for its potential skin-protective properties against UV-induced damage. Researchers utilize this compound in studying phenolic ester metabolism and as a precursor for polymer and material science applications.

Safety and Hazards

GHS Hazard Statements

• H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

Precautionary Statements

• P264, P270, P301+P317, P330, and P501

Hazard Classes and Categories

• Acute Tox. 4 (100%)

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