18982-18-8

Basic information

• Product Name: 4-HYDROXYBENZOIC ACID ALLYL ESTER
• Synonyms: ALLYLPARABEN;ALLYL 4-HYDROXYBENZOATE;4-HYDROXYBENZOIC ACID ALLYL ESTER;4-Hydroxybenzoic acid 2-propenyl ester;p-Hydroxybenzoic acid allyl ester;Allyl 4-Hydroxybenzoic acid;Allylparaben 4-Hydroxybenzoic Acid Allyl Ester;Benzoic acid, 4-hydroxy-, 2-propen-1-yl ester
• CAS NO: 18982-18-8
• Molecular Formula: C₁₀H₁₀O₃
• Molecular Weight: 178.18
• Mol File: 18982-18-8.mol
• Article Data: 15

Chemical Properties

• Melting Point: 103 °C
• Boiling Point: 310.2°C at 760 mmHg
• Flash Point: 134.8°C
• Appearance: /
• Density: 1.158g/cm³
• Vapor Pressure: 0.000334mmHg at 25°C
• Refractive Index: 1.548
• Solubility: soluble in Methanol
• PKA: 8.14±0.15(Predicted)
• CAS DataBase Reference: 4-HYDROXYBENZOIC ACID ALLYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-HYDROXYBENZOIC ACID ALLYL ESTER(18982-18-8)
• EPA Substance Registry System: 4-HYDROXYBENZOIC ACID ALLYL ESTER(18982-18-8)

Safety Data

• Hazardous Substances Data: 18982-18-8(Hazardous Substances Data)

Usage

General Description

4-Hydroxybenzoic acid allyl ester is a chemical compound that belongs to the family of allyl esters. It is commonly used in the manufacturing of fragrances, flavors, and other aromatic compounds. It is known for its characteristic sweet, floral, and slightly spicy odor. This chemical is also used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it is a versatile chemical building block that can be further modified to create different derivatives with unique properties and applications. Overall, 4-hydroxybenzoic acid allyl ester is a valuable compound in the chemical industry with a wide range of uses.

InChI:InChI=1/C10H10O3/c1-2-7-13-10(12)8-3-5-9(11)6-4-8/h2-6,11H,1,7H2

Upstream product

• 107-18-6 allyl alcohol 
• 99-96-7 4-hydroxy-benzoic acid 
• 106-95-6 allyl bromide 
• 28141-24-4 4-hydroxybenzoyl chloride 
• 591-87-7 Allyl acetate 
• 7732-18-5 water 
• 584-08-7 potassium carbonate 
• 2345-34-8 4-acetyloxy-benzoic acid 
• 27914-73-4 4-acetoxybenzoyl chloride 
• 100519-08-2 allyl 4-acetoxybenzoate 
• 107-05-1 3-chloroprop-1-ene 

Downstream Products

• 26595-60-8 allyl (4-allyloxy)benzoate 
• 70193-37-2 4-[3-(4-Chloro-phenoxy)-2-oxo-propoxy]-benzoic acid allyl ester 
• 60377-00-6 4-[3-(4-Chloro-phenoxy)-2-hydroxy-propoxy]-benzoic acid allyl ester 
• 70193-76-9 4-[3-(4-Isopropyl-phenoxy)-2-oxo-propoxy]-benzoic acid allyl ester 
• 70193-58-7 4-[3-(4-Bromo-phenoxy)-2-oxo-propoxy]-benzoic acid allyl ester 
• 70193-63-4 3-{4-[3-(4-Bromo-phenoxy)-2-oxo-propoxy]-phenyl}-propionic acid allyl ester 
• 70193-85-0 4-[3-(4-tert-Butyl-phenoxy)-2-oxo-propoxy]-benzoic acid allyl ester 
• 142504-49-2 benzyl 11-<4-(allyloxycarbonyl)phenyloxy>undecanoate 
• 142504-48-1 benzyl <2-<2-<2-<4-(allyloxycarbonyl)phenyloxy>ethoxy>ethoxy>ethoxy>acetate 
• 91061-33-5 2-ethoxy-1-(4-hydroxyphenyl)ethan-1-one 
• 137524-65-3 1-(4-hydroxyphenyl)-2-phenylthioethanone 
• 100866-41-9 1-(4-hydroxyphenyl)-2-phenylaminoethanone 
• 131179-71-0 4-<(anilinocarbonyl)methyl>phenol 
• 27727-37-3 benzyl p-hydroxyphenylacetate 

Relevant articles and documents

METHOD FOR MANUFACTURING P-HYDROXY BENZOIC ACID ALLYL POLYMER

PROBLEM TO BE SOLVED: To provide a method for efficiently manufacturing p-hydroxy benzoic acid allyl polymer having high antibacterial property. SOLUTION: There is provided a method for manufacturing p-hydroxy benzoic acid allyl polymer including (A) a pr

A simple FRET-based modular design for diagnostic probes

In recent years, there has been a massive effort to develop molecular probes with optical modes of action. Probes generally produce detectable signals based on changes in fluorescence properties. Here, we demonstrate the potential of self-immolative molecular adaptors as a platform for Turn-On probes based on the FRET technique. The probe is equipped with identical fluorophore pairs or a fluorophore/quencher FRET pair and a triggering substrate. Upon reaction of the analyte of interest with the triggering substrate, the self-immolative adaptor spontaneously releases the two dye molecules to break off the FRET effect. As a result, a new measurable fluorescent signal is generated. The fluorescence obtained can be used to quantify the analyte. The modular structure of the probe design will allow the preparation of various chemical probes based on the FRET activation technique.

Synthesis of para-substituted bicyclo[2.2.1]hept-5-en-2-ylmethyl benzoates

para-Substituted bicyclo[2.2.1]hept-5-en-2-ylmethyl benzoates were synthesized by the Diels-Alder reaction of cyclopentadiene with the corresponding para-substituted allyl benzoates, and optimal reaction conditions were found. The product structure was confirmed by independent synthesis and IR and 1H NMR spectroscopy.