82304-99-2

Basic information

• Product Name: 3-Formyl-4-hydroxybenzoic acid ethyl ester
• Synonyms: Ethyl 3-formyl-4-hydroxybenzoate;3-Formyl-4-hydroxybenzoic acid ethyl ester
• CAS NO: 82304-99-2
• Molecular Formula: C₁₀H₁₀O₄
• Molecular Weight: 194
• Mol File: 82304-99-2.mol
• Article Data: 6

Chemical Properties

• Melting Point: 104-106℃
• Boiling Point: 313℃
• Flash Point: 123℃
• Appearance: /
• Density: 1.261
• Vapor Pressure: 0.000286mmHg at 25°C
• Refractive Index: 1.58
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-Formyl-4-hydroxybenzoic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Formyl-4-hydroxybenzoic acid ethyl ester(82304-99-2)
• EPA Substance Registry System: 3-Formyl-4-hydroxybenzoic acid ethyl ester(82304-99-2)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 3
• Hazardous Substances Data: 82304-99-2(Hazardous Substances Data)

Usage

General Description

3-Formyl-4-hydroxybenzoic acid ethyl ester, often referred to as ethyl 3-(4-hydroxy-3-formylphenyl)propanoate, is a chemical compound with the molecular formula C11H12O4. It is a derivative of salicylic acid, commonly used in the pharmaceutical and cosmetic industries. 3-Formyl-4-hydroxybenzoic acid ethyl ester is known for its antioxidant and anti-inflammatory properties, and it is widely used in skincare products and topical medications. Additionally, it has potential applications in the field of organic synthesis and drug development due to its unique chemical structure and pharmacological properties. Overall, 3-Formyl-4-hydroxybenzoic acid ethyl ester is an important chemical compound with various potential uses in the pharmaceutical and cosmetic industries.

InChI:InChI=1/C10H10O4/c1-2-14-10(13)7-3-4-9(12)8(5-7)6-11/h3-6,12H,2H2,1H3

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 50-00-0 formaldehyd 
• 64-17-5 ethanol 
• 584-87-2 3-formyl-4-hydroxybenzoic acid 
• 100-97-0 hexamethylenetetramine 

Downstream Products

• 1360060-12-3 ethyl 3-[(E)-2-(4-chlorophenyl)vinyl]-4-hydroxybenzoate 
• 858124-17-1 ethyl (E)-3-[2-(4-chlorophenyl)vinyl]-4-methoxybenzoate 
• 1374791-85-1 3-[(E)-2-(4-chlorophenyl)vinyl]-4-methoxy-benzoyl chloride 
• 858124-06-8 5-ethoxycarbonyl-2-methoxybenzoic acid 
• 858124-09-1 ethyl 3-[(4-chlorophenyl)carbamoyl]-4-methoxybenzoate 
• 858124-10-4 3-[(4-chlorophenyl)carbamoyl]-4-methoxybenzoic acid 
• 1360060-63-4 ethyl 3-[(E)-2-(4-chlorophenyl)vinyl]-4-ethoxybenzoate 
• 1360060-64-5 ethyl 3-[(E)-2-(4-chlorophenyl)vinyl]-4-propoxybenzoate 
• 1360060-55-4 3-[(E)-2-(4-chlorophenyl)vinyl]-4-propoxybenzamide 
• 1360060-57-6 3-[(E)-2-(4-chlorophenyl)vinyl]-4-[2-(2-hydroxyethoxy)ethoxy]benzamide 
• 1360060-59-8 3-[(E)-2-(4-chlorophenyl)vinyl]-4-(2-dimethylaminoethoxy)benzamide 
• 1360060-61-2 3-[(E)-2-(4-chlorophenyl)vinyl]-4-[2-(4-methylpiperazin-1-yl)ethoxy]benzamide 
• 858124-18-2 3-[(E)-2-(4-chlorophenyl)vinyl]-4-methoxybenzoic acid 

Relevant articles and documents

CARBOXAMIDE AND SULFONAMIDE DERIVATIVES USEFUL AS TEAD MODULATORS

The invention is concerned with the compounds of formula (I) and formula (II): and pharmaceutically acceptable salts thereof. In addition, the present invention relates to methods of using the compounds of formula (I) and formula (II) as well as pharmaceutical compositions containing such compounds. The compounds are useful in treating diseases and conditions mediated by TEAD, such as cancer.

Angiogenesis inhibitors identified by cell-based high-throughput screening: Synthesis, structure-activity relationships and biological evaluation of 3-[(E)-styryl]benzamides that specifically inhibit endothelial cell proliferation

Proliferation of endothelial cells is critical for angiogenesis. We report orally available, in vivo active antiangiogenic agents which specifically inhibit endothelial cell proliferation. After identifying human umbilical vein endothelial cell (HUVEC) pr

An efficient one-pot synthesis of pyrrolo[4,3,2-ij]isoquinoline derivatives by a consecutive aza-wittig/electrocyclic ring-closure/intramolecular acylation process

Iminophosphorane, ethyl 5-ethoxycarbonyl-2-methoxy-α-[(triphenylphosphoranylidene)amino]cinn amate (4) reacts with aliphatic and aromatic isocyanates in toluene at 170°C to give directly the corresponding pyrrolo[4,3,2-ij]isoquinolines 8 in moderate yields.