30379-54-5

Basic information

• Product Name: Benzyl Benzyloxyacetate
• Synonyms: Benzyl Benzyloxyacetate;2-(PhenylMethoxy)acetic Acid PhenylMethyl Ester;NSC 153413;Benzyl 2-(benzyloxy)acetate
• CAS NO: 30379-54-5
• Molecular Formula: C₁₆H₁₆O₃
• Molecular Weight: 256
• Product Categories: Aromatics;Miscellaneous Reagents
• Mol File: 30379-54-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 386.4°C at 760 mmHg
• Flash Point: 138.6°C
• Appearance: /
• Density: 1.135g/cm³
• Vapor Pressure: 3.54E-06mmHg at 25°C
• Refractive Index: 1.56
• CAS DataBase Reference: Benzyl Benzyloxyacetate(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl Benzyloxyacetate(30379-54-5)
• EPA Substance Registry System: Benzyl Benzyloxyacetate(30379-54-5)

Safety Data

• Hazardous Substances Data: 30379-54-5(Hazardous Substances Data)

Usage

General Description

Benzyl benzyloxyacetate is an organic compound commonly used in the fragrance industry as a synthetic scent ingredient. It is a derivative of benzoic acid and benzyl alcohol, and is also known by the trade name "Benzyl phenylacetate". This chemical is often used as a fixative in perfumes and as a flavoring agent in the food industry. It has a sweet, floral, and slightly fruity odor, making it a popular choice for adding a pleasant aroma to various products. However, it is important to use this chemical with caution as it may cause skin and eye irritation and should be handled and stored properly.

InChI:InChI=1/C16H16O3/c17-16(19-12-15-9-5-2-6-10-15)13-18-11-14-7-3-1-4-8-14/h1-10H,11-13H2

Upstream product

• 140-18-1 Benzyl chloroacetate 
• 20194-18-7 sodium phenyl-methanolate 
• 30379-55-6 benzyloxyacetic acid 
• 60656-87-3 benzyloxyacetoaldehyde 
• 100-51-6 benzyl alcohol 
• 5437-45-6 Benzyl bromoacetate 
• 105-39-5 chloroacetic acid ethyl ester 
• 96-34-4 methyl chloroacetate 
• 105-36-2 ethyl bromoacetate 
• 132565-90-3 4-O-benzoyl-2,3:5,6-di-O-isopropylidene-D-mannose 
• 132565-91-4 <(Benzyloxy)(benzyloxycarbonyl)methyl>triphenylphosphonium Bromide 

Downstream Products

• 854626-40-7 4-benzyloxy-2-phenyl-acetoacetonitrile 
• 30379-55-6 benzyloxyacetic acid 
• 389130-71-6 ethyl 5-(benzyloxy)-2-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate 
• 389130-69-2 tris[(2,3-dimethyl-5-benzyloxy-6-carboxamido-4-pyrimidinone)ethyl]amine 
• 389130-68-1 2,3-dimethyl-5-benzyloxy-6-carboxy-4-pyrimidinone 
• 389130-72-7 2,3-dimethyl-5-benzyloxy-6-carboxy-4-pyrimidinone ethyl ester 
• 1092454-10-8 4-(benzyloxy)-1-phenylbutane-1,3-dione 
• 131066-97-2 benzyl 2-(benzyloxy)-3-cyclopropyl-3-hydroxybutanoate 
• 30502-34-2 O-(O'-Benzylglykoloyl)glykolsaeure-benzylester 

Relevant articles and documents

A novel VIVO-pyrimidinone complex: Synthesis, solution speciation and human serum protein binding

The pyrimidinones mhcpe, 2-methyl-3H-5-hydroxy-6-carboxy-4-pyrimidinone ethyl ester (mhcpe, 1), 2,3-dimethyl-5-benzyloxy-6-carboxy-4-pyrimidinone ethyl ester (dbcpe, 2) and N-methyl-2,3-dimethyl-5-hydroxy-6-carboxyamido-4- pyrimidinone (N-MeHOPY, 3), are

Synthesis of 3-Deoxy-D-manno-2-octulosonic Acid (KDO)

triphenylphosphonium bromide (8), obtained from glyoxylic acid via a convenient one-pot procedure, reacted in a Wittig reaction with 4-O-benzyl-2,3:5,6-di-O-isopropylidene-D-mannose (7), readily synthesized on a large

Photolysis of Alkoxyacetic Acids in the presence of Mercury(II) Oxide and Iodine

Homolytic decarboxylation of a series of alkoxyacetic acids has furnished alkoxyalkyl alkoxyacetates when no substituents were present at the 2-position.Electron donating and withdrawing 2-substituents, with the exception of trichloromethyl, afforded products due to fragmentation of the alkoxyacetic acids.The reaction pathway is rationalised on the basis of the reactivity of the alkoxyalkyl iodide intermediates.