5842-49-9

Usage

Physical state

Colorless liquid

Odor

Strong fruity

Usage in fragrance and flavor industry

Component in perfumes, soaps, air fresheners, and flavoring agent in food and beverages

Potential use

Bio-based solvent in industrial applications

Antimicrobial properties

Potential candidate for use in pharmaceutical and healthcare products

Safety precautions

Volatile organic compound, handle and store with proper precautions to minimize exposure and potential health risks.

Upstream product

• 78-84-2 isobutyraldehyde 
• 918-79-6 3-hydroxy-2,2,4-trimethyl-pentanal 
• 75-24-1 trimethylaluminum 
• 74-99-7 prop-1-yne 
• 5863-13-8 ethyl 2,2-dimethyl-3-phenoxycyclopropane-1-carboxylate 
• 59211-16-4 2,2,4-trimethyl-pent-3-enoic acid ethyl ester 
• 7403-65-8 ethyl 2,2,4-trimethyl-3-hydroxyvalerate 
• 108-24-7 acetic anhydride 
• 764-51-2 Bis(2-methylprop-1-enyl) ether 
• 5530-15-4 2,2,4,4-tetramethyl-cyclobutane-1,3-dione bis-[(toluene-4-sulfonyl)-hydrazone] 
• 5842-47-7 2-(2,2-dimethyl-3-phenoxy-cyclopropyl)-propan-2-ol 
• 10477-54-0 2,2,4,4-tetramethyl-3c-(toluene-4-sulfonyloxy)-cyclobutan-r-ol 
• 10477-53-9 2,2,4,4-tetramethyl-3t-(toluene-4-sulfonyloxy)-cyclobutan-r-ol 
• 3010-96-6 2,2,4,4-tetramethylcyclobutane-1,3-diol 

Downstream Products

• 5842-53-5 2,2,4-trimethyl-pent-3-en-1-ol 
• 4177-03-1 2,2,4-Trimethyl-pent-3-ensaeure 
• 24512-85-4 5,5,7-trimethyl-octa-3t,6-dien-2-one 
• 110835-91-1 2,2,4-trimethyl-1-phenylpent-3-en-1-ol 
• 74157-94-1 2,2,4-trimethyl-1-phenylpent-3-en-1-one 
• 110835-92-2 (E)-N-methoxy 2,2,4-trimethyl-1-phenylpent-3-1-imine 
• 5863-17-2 2,2,4-Trimethyl-pent-3-en-1-ol-(3,5-dinitro-benzoesaeureester) 
• 14224-28-3 2.2.4-Trimethyl-pent-3-en-1-ol-p-toluolsulfonsaeure-ester 

Relevant academic research and scientific papers

An aprotic Tamao oxidation/syn-selective tautomerization reaction for the efficient synthesis of the C(1)-C(9) fragment of fludelone

An efficient synthesis of the C(1)-C(9) fragment of fludelone has been developed. The key step is a tandem silylformylation-crotylsilylation/ Tamao oxidation sequence that establishes the C(5) ketone, the C(6), C(7), and C(8) stereocenters, and the C(9) alkene in a single operation from a readily accessed starting material. The stereochemical outcome at C(6) depends critically on the development of an aprotic Tamao oxidation, which leads to a reversal in the intrinsic diastereoselectivity observed using standard Tamao oxidation conditions.

Chemoselective synthesis of 1,1-diacetates from aldehydes in the presence of Al(HSO4)3 under mild solvent-free conditions

A novel efficient procedure has been developed for the preparation of acylals in high yields by reaction of the corresponding aldehydes with acetic anhydride in the presence of Al(HSO4)3 as catalyst under mild (room temperature) solvent-free conditions.

PHOTOCHEMISTRY OF BIS(2-METHYL-1-PROPENYL)ETHER AND 2,2,4,4-TETRAMETHYL-6-OXABICYCLOHEXAN-3-ONE: ON THE SEARCH FOR THE OXYDI-?-METHANE REARRANGEMENT

?,?*-Excitation of bis(2-methyl-1-propenyl)ether leads to products derived from a vinyl-vinyloxy radical pair; photochemical decarbonylation (n,?*) of the title ketone provides an entry into the diradical manifold of the oxydi-?-methane rearrangement.