18982-18-8 Usage
Description
4-Hydroxybenzoic acid allyl ester is a versatile chemical compound belonging to the family of allyl esters. It is characterized by its sweet, floral, and slightly spicy odor, making it a valuable component in the creation of fragrances, flavors, and other aromatic compounds. 4-HYDROXYBENZOIC ACID ALLYL ESTER also serves as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals, showcasing its importance in the chemical industry.
Uses
Used in Fragrance and Flavor Industry:
4-Hydroxybenzoic acid allyl ester is used as a key ingredient in the formulation of fragrances and flavors for its distinctive sweet, floral, and slightly spicy aroma, enhancing the sensory experience of various consumer products.
Used in Pharmaceutical Industry:
As an intermediate in the synthesis of pharmaceuticals, 4-hydroxybenzoic acid allyl ester plays a crucial role in the development of new drugs, contributing to advancements in healthcare and medicine.
Used in Agrochemical Industry:
In the agrochemical sector, 4-hydroxybenzoic acid allyl ester is utilized as a building block for the synthesis of various agrochemicals, aiding in the production of effective and innovative agricultural products.
Used in Fine Chemicals Industry:
4-HYDROXYBENZOIC ACID ALLYL ESTER is employed as an intermediate in the production of fine chemicals, where its unique properties and reactivity contribute to the creation of high-quality specialty chemicals for diverse applications.
Used in Chemical Synthesis:
4-Hydroxybenzoic acid allyl ester serves as a versatile chemical building block, allowing for further modification to create different derivatives with unique properties and applications, expanding its utility across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 18982-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,8 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18982-18:
(7*1)+(6*8)+(5*9)+(4*8)+(3*2)+(2*1)+(1*8)=148
148 % 10 = 8
So 18982-18-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O3/c1-2-7-13-10(12)8-3-5-9(11)6-4-8/h2-6,11H,1,7H2
18982-18-8Relevant articles and documents
Production of carboxylic acid and carboxylic acid ester allylation intermediate
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Paragraph 0071; 0072, (2019/06/04)
The invention discloses a preparation method of aryl/alkyl carboxylic acid which serves as a useful intermediate of a polymerized liquid crystal compound and is provided with (methyl) propene acyloxy, and aryl/alkyl allyl carboxylate which serves as an in
A simple FRET-based modular design for diagnostic probes
Redy, Orit,Kisin-Finfer, Einat,Sella, Eran,Shabat, Doron
supporting information; scheme or table, p. 710 - 715 (2012/02/05)
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
Mamedbeili,Kyazimova,Nagiev,Abdiev,Aliev
experimental part, p. 74 - 77 (2009/07/17)
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.
