77513-40-7

Usage

Uses

Used in Food Industry:
Benzoic acid, 3-hydroxy-, phenylmethyl ester is used as a flavoring agent and preservative in processed foods to enhance taste and extend shelf life by inhibiting the growth of bacteria and fungi.
Used in Cosmetic Industry:
It is used as a fragrance component in perfumes, lotions, and soaps, adding a pleasant scent to these products.
Used in Pharmaceutical Industry:
Benzoic acid, 3-hydroxy-, phenylmethyl ester is used as a preservative in pharmaceutical products to prevent microbial contamination and ensure product safety and efficacy.
Used in Organic Synthesis:
This chemical compound serves as a precursor in organic synthesis, contributing to the production of various pharmaceuticals and other chemical products.
However, it is important to use Benzoic acid, 3-hydroxy-, phenylmethyl ester with caution, as it can cause skin and eye irritation at high concentrations.

Upstream product

• 100-39-0 benzyl bromide 
• 144-55-8 sodium hydrogencarbonate 
• 99-06-9 3-Carboxyphenol 
• 437614-09-0 3-Methoxy-2-vinyl-benzoic acid 3-benzyloxycarbonyl-phenyl ester 
• 437614-10-3 2-Formyl-3-methoxy-benzoic acid 3-benzyloxycarbonyl-phenyl ester 
• 100-44-7 benzyl chloride 

Downstream Products

• 869881-36-7 3-chlorooxalyloxy-benzoic acid benzyl ester 
• 760175-60-8 biphenyl-4-carboxylic acid 3-benzyloxycarbonyl-phenyl ester 
• 912296-82-3 3-(benzyloxycarbonyl)phenyl chloroformate 
• 912296-74-3 3-(2-Methoxy-2-phenylacetylamino-acetoxy)-benzoic acid benzyl ester 
• 912296-78-7 3-(3-benzyloxycarbonylamino-2-phenylacetylamino-propionyloxy)-benzoic acid benzyl ester 
• 269071-62-7 5-(2-Adamantan-1-yl-ethyl)-2-o-tolyl-1H-imidazole-4-carboxylic Acid 3-benzyloxycarbonyl-phenyl Ester 
• 1208236-42-3 benzyl 3-[2-(N-methyl-benzylaminocarbonyl)-ethanoyl]-oxybenzoate 
• 1208236-43-4 benzyl 3-[2-(N,N-dibenzylaminocarbonyl)-ethanoyl]-oxybenzoate 
• 1208236-26-3 3-(2-benzylcarbamoyl-propionyloxy)-benzoic acid benzyl ester 
• 1208236-30-9 3-benzyloxycarbonylphenyl 1-benzyl-2-oxo-pyrrolidine-3-carboxylate 
• 1208236-36-5 3-benzyloxycarbonylphenyl N-benzyl-2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxylate 
• 1208236-29-6 3-benzyloxycarbonylphenyl N-benzyl-2-methoxymalonamate 
• 940963-70-2 benzyl (2RS,R_PS_P)-2-benzyloxycarbonylamino-4-{[3-(benzyloxycarbonyl)phenoxy](methoxy)phosphoryl}butanoate 
• 437614-09-0 3-Methoxy-2-vinyl-benzoic acid 3-benzyloxycarbonyl-phenyl ester 

Relevant academic research and scientific papers

A simple and effective synthesis of 3- And 4-((Phenylcarbamoyl)oxy)benzoic acids

Phenserine, posiphen, tolserine and cymserine and its derivatives are experimental Alzheimer's disease drugs that contain a phenyl phenylcarbamate moiety that is responsible for their anti-Alzheimer activities. We have developed a simple (3 steps) and effective (overall yields 76-90%) method for preparing 3- and 4-((phenylcarbamoyl)oxy)benzoic acids which can be reacted with amines to produce phenyl phenylcarbamate moiety containing amides as new potential anti-Alzheimer disease drugs. The synthesized carboxylic acids are thus important building blocks with potential use in medicinal chemistry and drug discovery.

Phosphonate-based irreversible inhibitors of human γ-glutamyl transpeptidase (GGT). GGsTop is a non-toxic and highly selective inhibitor with critical electrostatic interaction with an active-site residue Lys562 for enhanced inhibitory activity

γ-Glutamyl transpeptidase (GGT, EC 2.3.2.2) that catalyzes the hydrolysis and transpeptidation of glutathione and its S-conjugates is involved in a number of physiological and pathological processes through glutathione metabolism and is an attractive phar

NOVEL COMPOUNDS AND THEIR USE IN THERAPY

The invention provides compounds which inhibit N-myristoyltransferase and are selective for protozoal N-myristoyltransferase and, consequently suitable to treat microbial infections, including viral and fungal infections, and protozoan infections such as malaria, leishmaniasis and sleeping sickness.

Chemoselective esterification of phenolic acids in the presence of sodium bicarbonate in ionic liquids

Chemoselective esterification of phenolic acids with dialkyl sulphates or alkyl halides in the presence of sodium bicarbonate in 1,3-dialkylimidazolium ionic liquids is reported in excellent yields and less reaction time as compared to organic solvents. Copyright Taylor & Francis Group, LLC.

Process for the preparation of carboxylic benzyl esters

Carboxylic benzyl esters can be prepared by reacting benzyl chloride with carboxylic acids in the presence of one or more quaternary ammonium carboxylates as catalyst.

Formal total synthesis of the PKC inhibitor, balanol: Preparation of the fully protected benzophenone fragment

The synthesis of a perbenzylated derivative of balanol's highly functionalized benzophenone fragment is reported employing a regioselective Heck reaction as the key step for the connection of the two aromatic rings. The intermediate 7-membered lactone obt

ANTITHROMOBOTIC AGENTS

This invention relates to L-arginine aldehyde derivatives, having the Formula I STR1 where X and Y have the values defined in the description, as well as pharmaceutical formulations containing those compounds and methods of their use as thrombin inhibitors, coagulation inhibitors, and thromboembolic disorder agents.