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Usage

Uses

Used in Fragrance Industry:
BENZYLOXYACETALDEHYDE DIETHYL ACETAL is used as a fragrance ingredient for its sweet, floral scent, contributing to the overall aroma profile in perfumes, soaps, and cosmetics. Its unique olfactory characteristics enhance the sensory experience of these products.
Used in Flavor Industry:
In the food and beverage sector, BENZYLOXYACETALDEHYDE DIETHYL ACETAL is used as a food flavoring to impart a subtle sweetness and floral note to various products, enhancing their taste and appeal to consumers.
Used as a Solvent in Chemical Reactions:
BENZYLOXYACETALDEHYDE DIETHYL ACETAL also serves as a solvent in chemical processes, facilitating reactions and aiding in the synthesis of other compounds. Its stability under normal conditions makes it a reliable choice for such applications.
Overall, BENZYLOXYACETALDEHYDE DIETHYL ACETAL is a multifaceted chemical compound that finds use in a variety of applications across different industries, primarily due to its sensory attributes and chemical properties. When used according to safety guidelines, it is considered to be a relatively safe and effective ingredient.

InChI:InChI=1/C13H20O3/c1-3-15-13(16-4-2)11-14-10-12-8-6-5-7-9-12/h5-9,13H,3-4,10-11H2,1-2H3

Upstream product

• 100-39-0 benzyl bromide 
• 621-63-6 glycoaldehyde diethyl acetal 
• 2032-35-1 Bromoacetaldehyde diethyl acetal 
• 100-51-6 benzyl alcohol 

Downstream Products

• 103036-14-2 2-benzyloxy-1,1-bis-(4-hydroxy-2-oxo-2H-chromen-3-yl)-ethane 
• 94776-62-2 1-Amino-2-hydroxyethane-P-methylphosphinic acid 
• 70350-62-8 phosphonylethanolamine 
• 119117-64-5 1,2,2-tribenzyloxyethane 
• 216011-87-9 5-benzyloxy-3-(4-methyl-thiazol-2-yl)-1H-pyridin-2-one 
• 229184-02-5 5-benzyloxy-1-(2-bromo-benzyl)-3-(4-methyl-thiazol-2-yl)-1H-pyridin-2-one 
• 216012-93-0 5-Benzyloxy-1-(4-bromopyridin-3-ylmethyl)-3-(4-methylthiazol-2-yl)-1H-pyridin-2-one 
• 229184-03-6 5-benzyloxy-1-[2-(2-bromo-phenyl)-ethyl]-3-(4-methyl-thiazol-2-yl)-1H-pyridin-2-one 
• 229184-04-7 5-benzyloxy-1-[2-(3-bromo-pyridin-4-yl)-ethyl]-3-(4-methyl-thiazol-2-yl)-1H-pyridin-2-one 
• 216012-90-7 5-benzyloxy-1-[3-(3-bromo-pyridin-4-yl)-propyl]-3-(4-methyl-thiazol-2-yl)-1H-pyridin-2-one 
• 104048-40-0 3-Benzyloxymethyl-5-vinyl-4,5-dihydro-isoxazole 
• 104048-51-3 (S)-1-((S)-3-Benzyloxymethyl-4,5-dihydro-isoxazol-5-yl)-ethane-1,2-diol 
• 104048-51-3 (R)-1-((S)-3-Benzyloxymethyl-4,5-dihydro-isoxazol-5-yl)-ethane-1,2-diol 
• 1065609-84-8 2-(4-(benzyloxy)-1H-pyrazol-1-yl)ethanol 

Relevant academic research and scientific papers

Synthesis of three selectively deuterated propylene oxides

Three different selectively deuterated propylene oxides have been synthesized for use in quasi-elastic neutron scattering studies of the dynamics of propylene oxide within clathrate hydrate cages. Copyright 2011 John Wiley & Sons, Ltd. Three different selectively deuterated propylene oxides have been synthesized for use in quasi-elastic neutron scattering studies of the dynamics of propylene oxide within clathrate hydrate cages. Copyright

Process for Manufacture of Optically Active 2-(Acyloxymethyl)-1,3-Oxathiolanes

There is provided a process for manufacture of optically-active, 2-(acyloxymethyl)-1,3-oxathiolanes of Formula I comprising a preparation of a racemic compound and an enzyme-catalyzed kinetic resolution of the enantiomers. The invention may further provide for the esterification and racemization of the by-product of the enzymatic reaction. In this manner, 2(R)-(benzoyloxymethyl)-1,3-oxathiolane is prepared as a useful intermediate for manufacture of the anti-HIV drug Apricitabine.

Synthesis and biological evaluation of 3-hydroxymethylpyrimido[1,6-c][1,3]oxazine derivatives

A number of 5-substituted 3-hydroxymethylpyrimido[1,6-c] [1,3]-oxazine derivatives were synthesized and evaluated for their biological activity. Compound (10) showed slight activity (GI50 = 2.7 μM) against MDA-MB-231/ATTC Breast Cancer cell line.

COBALT-MEDIATED ALKYLATION OF SILOXY FURANS

Dicobalt hexacarbonyl complexes of propargylium and α-vinylpropargylium cations couple efficiently with 2-trimethylsiloxyfuran (5), 4-trimethylsilyloxy-2-benzyloxymethylfuran (15) and 2-trimethylsilyl-3-trimethylsilyloxy-4-ethylbenzofuran (20) to produce the corresponding complexed furan derivatives in good yields.A convenient procedure for introducing the 2,4-enyne moiety regio- and stereoselectively into the above heterocycles using this methodology is described.

Analogues of the Antiviral Acyclonucleoside 9-(4-Hydroxy-3-hydroxymethylbutyl)guanine. Part 1. Substitutions on C-2' of the Acyclic N-9 Substituent

Syntheses of 9-(4-hydroxy-3-hydroxymethyl-2-methylbutyl)guanine (4), 9-(4-hydroxy-3-hydroxymethyl-2-methoxybutyl)guanine (5), 9-guanine (6), 9-(2,4-dihydroxy-3-hydroxymethylbutyl)guanine (7), and 9-(2-fluoro-4-hydrox

Degradation Pathway of Arylglycerol-β-aryl Ethers by Phanerochaete chrysosporium

The degradation pathway for the most important β-O-4 lignin substructure with a white rot fungus, Phanerochaete chrysosporium, was investigated, and the following conclusions were obtained. a) The allyl alcohol end group attached to the β-O-4 substructure was degraded to a formyl group via a glycerol group. b) Arylglycerol was formed by the cleavage of the β-O-4 substructure without involvement of the hydroxylation reaction at Cβ. c) 18O was not incorporated from 18O2 into arylglycerol nor phenol liberated by the degradation of the β-O-4 substrucrure, but was incorporated into the benzyl alcohol derivative formed by Cα-Cβ cleavage. d( Two alternative degradation pathway of the β-O-4 substructure, a pathway via arylglycerol and direct oxygenative Cα-Cβ cleavage, are proposed