69033-81-4

69033-81-4 - Names and Identifiers

Name	4-Propoxycinnamic acid
Synonyms	TIMTEC-BB SBB002371 RARECHEM BK HW 0039 4-PROPOXYCINNAMIC ACID 4-Propoxycinnamic acid 3-(4-PROPOXYPHENYL)ACRYLIC ACID (Z)-3-(4-propoxyphenyl)acrylic acid (E)-3-(4-Propoxyphenyl)acrylic acid (2E)-3-(4-Propoxyphenyl)acrylic acid (2E)-3-(4-propoxyphenyl)prop-2-enoic acid 3-(4-Propoxyphenyl)acrylic acid, 3-(4-Propoxyphenyl)prop-2-enoic acid
CAS	69033-81-4
InChI	InChI=1/C12H14O3/c1-2-9-15-11-6-3-10(4-7-11)5-8-12(13)14/h3-8H,2,9H2,1H3,(H,13,14)/b8-5+
InChIKey	WTYNDSOJMSGRQV-VMPITWQZSA-N

69033-81-4 - Physico-chemical Properties

Molecular Formula	C12H14O3
Molar Mass	206.24
Density	1.132g/cm³
Melting Point	166.0 to 172.0 °C
Boling Point	364.8°C at 760 mmHg
Flash Point	140.4°C
Vapor Presure	5.82E-06mmHg at 25°C
Appearance	Crystalline powder
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.569

69033-81-4 - Risk and Safety

Hazard Symbols	Xi - Irritant
Hazard Class	IRRITANT

69033-81-4 - Introduction

4-Propoxycinnamic acid, also known as 4-Propoxycinnamic acid, is an organic compound whose chemical formula is C12H12O3. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
-Appearance: 4-Propoxycinnamic acid exists in the form of white to light yellow crystals or crystalline powder.
-Solubility: It is almost insoluble in water, soluble in ether, chloroform, alcohols and organic solvents.

Use:
-Chemical research: 4-Propoxycinnamic acid can be used as an intermediate in organic synthesis and used in the synthesis of other organic compounds.
-Preservative: It can also be used as a preservative in food and beverages to extend its shelf life.
-Pharmaceutical applications: Some studies have shown that 4-Propoxycinnamic acid may have antibacterial, antioxidant, anti-inflammatory and anti-tumor activities, so it also has certain application prospects in the field of medicine.

Preparation Method:
4-Propoxycinnamic acid can be prepared by the following steps:
- 1. cinnamaldehyde reacts with propanol to generate 4-propoxy cinnamyl alcohol.
- 2.4-propoxy cinnamaldehyde was prepared by acid-catalyzed oxidation of 4-propoxy cinnamaldehyde.
- 3. Finally, 4-propoxycinnamic aldehyde is converted into 4-Propoxycinnamic acid through oxidation reaction.

Safety Information:
There is no definitive study or evaluation of the toxicity and safety of 4-Propoxycinnamic acid. As an organic compound, general laboratory practices such as wearing appropriate protective equipment and precautions should generally be followed. When using or handling the compound, all relevant safety guidelines and regulations should be observed. In all cases, the compound should be kept out of the reach of children. If necessary, professional safety information and operating instructions should be consulted before use.

Last Update：2024-04-09 02:00:47