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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.

18982-18-8

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18982-18-8 Usage

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

METHOD FOR MANUFACTURING P-HYDROXY BENZOIC ACID ALLYL POLYMER

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Paragraph 0049, (2017/02/24)

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

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.

(Meth)acrylate compound, curable composition using the same, curable composition for photo-nanoimprints, cured product of curable composition and method for manufacturing cured product

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Page/Page column 34, (2012/11/06)

It's object is to provide a (meth)acrylate compound excellent in photocurability, a curable composition comprising the compound and excellent in all of pattern accuracy, peelability, surface hardness, elasticity recovery and solvent resistance, an optical

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.

Synthesis and photostabilizing properties of hexachlorobicyclo[2.2.1]hept- 5-enylmethyl esters of substituted benzoic acids

Kyazimova,Mamedov,Babaev,Mamedova

, p. 438 - 442 (2008/09/20)

Polychlorinated bicyclic esters of p-substituted benzoic acids were prepared by the Diels-Alder reaction of hexachlorocyclopentadiene with allyl esters of p-substituted benzoic acids. Some of the adducts synthesized were tested as photostabilizers for polyethylene-based polymer formulations.

Synthesis of novel aromatic macrolactones via ring closing metathesis of substituted phenylalkanoic acid allylic esters

Brown, David P.,Duong, Hoan Q.

, p. 435 - 443 (2008/09/19)

(Chemical Equation Presented) Stable aromatic macrolactones have been synthesized and characterized from 2- and 3-substituted phenylalkanoic acid systems in modest yields.

Design and synthesis of phosphotyrosine peptidomimetic prodrugs

Garrido-Hernandez, Hugo,Moon, Kyung D.,Geahlen, Robert L.,Borch, Richard F.

, p. 3368 - 3376 (2007/10/03)

A novel approach to the intracellular delivery of aryl phosphates has been developed that utilizes a phosphoramidate-based prodrug approach. The prodrugs contain an ester group that undergoes reductive activation intracellularly with concomitant expulsion

Allylation of Alcohols and Carboxylic Acids with Allyl Acetate Catalyzed by [Ir(cod)2]+BF4- Complex

Nakagawa, Hideto,Hirabayashi, Tomotaka,Sakaguchi, Satoshi,Ishii, Yasutaka

, p. 3474 - 3477 (2007/10/03)

A facile method for the synthesis of allyl alkyl ethers from alcohols with allyl acetate was developed by the use of [Ir(cod)2] +BF4- complex. For instance, the reaction of allyl acetate with n-octyl alcohol in the presence of a catalytic amount of [Ir(cod)2]+BF4- complex afforded allyl octyl ether in quantitative yield. Allyl carboxylates were also prepared by the exchange reaction between carboxylic acids and allyl acetate in good yields. The [Ir(cod)2]+BF4- complex catalyzed the reaction of alkyl and aromatic amines with allyl acetate to lead to the corresponding allylamines in fair to good yields.

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