42783-78-8

Basic information

• Product Name: BENZYLOXYACETALDEHYDE DIETHYL ACETAL
• Synonyms: BENZYLOXYACETALDEHYDE DIETHYL ACETAL;1-BENZYLOXY-2,2-DIETHOXYETHANE;BENZYLOXYACETALDEHYDE DIETHYL ACETAL, 9;[(2,2-Diethoxyethoxy)Methyl]Benzene;1,1-Diethoxy-2-(benzyloxy)ethane;((2,2-Diethoxyethoxy)
• CAS NO: 42783-78-8
• Molecular Formula: C₁₃H₂₀O₃
• Molecular Weight: 224.3
• Product Categories: Acetals/Ketals/Ortho Esters;Organic Building Blocks;Oxygen Compounds
• Mol File: 42783-78-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 99-100 °C0.6 mm Hg(lit.)
• Flash Point: 175 °F
• Appearance: /
• Density: 0.987 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.00397mmHg at 25°C
• Refractive Index: n20/D 1.478(lit.)
• BRN: 3278795
• CAS DataBase Reference: BENZYLOXYACETALDEHYDE DIETHYL ACETAL(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYLOXYACETALDEHYDE DIETHYL ACETAL(42783-78-8)
• EPA Substance Registry System: BENZYLOXYACETALDEHYDE DIETHYL ACETAL(42783-78-8)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Safety Statements: 26-37
• WGK Germany: 3
• Hazardous Substances Data: 42783-78-8(Hazardous Substances Data)

Usage

General Description

Benzyloxyacetaldehyde diethyl acetal is a chemical compound used in the fragrance and flavor industry. It is a colorless liquid with a sweet, floral odor, and is commonly used as a fragrance ingredient in perfumes, soaps, and cosmetics. BENZYLOXYACETALDEHYDE DIETHYL ACETAL is also known for its use in the production of food flavorings and as a solvent in chemical reactions. It is considered to be relatively stable under normal conditions and is not known to pose significant health risks when used in accordance with safety guidelines.

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

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

Downstream Products

• 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 
• 1114830-03-3 C₁₄H₂₁N₂O⁽¹⁺⁾*F₆P^(1-) 
• 1400807-77-3 C₁₃H₁₄N₂O₂ 
• 866602-89-3 5-(benzyloxy)-2-cyclopropylpyrimidine 
• 1315317-80-6 1-(benzyloxy)(2,3,3,3-⁽²⁾H₄)propan-2-ol 
• 1315317-79-3 1-(benzyloxy)(3,3,3-⁽²⁾H₃)propan-2-one 
• 143462-35-5 3-(dimethylamino)-2-(phenylmethoxy)prop-2-enal 
• 855928-35-7 N-(1-benzyloxymethyl-2-cyclohex-1-enyl-2-nitro-ethyl)-acetamide 
• 854724-08-6 3-benzyloxy-1-cyclohex-1-enyl-1-nitro-propan-2-ol 
• 136015-13-9 2-(E-2-penten-4-ynyl)-5-benzyloxymethyl-2H-furan-3-one 

Relevant articles and documents

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

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.

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