2198-72-3

Usage

Uses

Used in Paints and Varnishes Industry:
4-N-PROPYL-4-HEPTANOL is used as a solvent for enhancing the solubility of various components in paint and varnish formulations, improving their application properties and performance.
Used in Perfumery:
4-N-PROPYL-4-HEPTANOL is used as a solvent in perfumes to dissolve and stabilize fragrance compounds, contributing to the longevity and intensity of the scent.
Used in Food and Beverage Industry:
4-N-PROPYL-4-HEPTANOL is used as a flavoring agent to impart specific taste and aroma characteristics to food and beverages, enhancing their sensory appeal.
Used in Chemical Synthesis:
4-N-PROPYL-4-HEPTANOL is used as a raw material in the synthesis of other chemicals, serving as a building block for the creation of various compounds with diverse applications.

InChI:InChI=1/C10H22O/c1-4-7-10(11,8-5-2)9-6-3/h11H,4-9H2,1-3H3

Upstream product

• 60-29-7 diethyl ether 
• 123-19-3 4-heptanone 
• 927-77-5 n-propylmagnesium bromide 
• 10557-57-0 propylmagnesium iodide 
• 155307-20-3 Ethyl 3-hydroxy-2,2-dimethyl-3-propylhexanoate 
• 2234-82-4 1-propylmagnesium chloride 
• 105-54-4 butanoic acid ethyl ester 
• 1619-62-1 2,2-dimethylmalonic acid diethyl ester 
• 75-44-5 phosgene 
• 4485-13-6 4-Propylhept-3-en 

Downstream Products

• 4485-13-6 4-Propylhept-3-en 
• 99862-75-6 4-chloro-4-propylheptane 
• 855412-21-4 4-(1,1-Dipropyl-butyl)-phenol 
• 121445-71-4 4-(1,1-Dipropylbutyl)-1,2-benzenediol 
• 718638-73-4 4-phenyl-4-propyl-heptane 
• 93816-24-1 4,4-dipropylundecane 
• 61822-36-4 4-propylheptan-4-amine 
• 17312-72-0 4,4-dipropylheptane 

Relevant academic research and scientific papers

Advanced procedure for the preparation of cis-1,2-dialkylcyclopropanols - Modified ate complex mechanism for titanium-mediated cyclopropanation of carboxylic esters with Grignard reagents

A procedure for the preparation of cis-1,2-dialkylcyclopropanols by titanium(IV) alkoxide-mediated cyclopropanarion of carboxylic esters with Grignard reagents, involving the addition of 1.5 equiv. of a higher homologue of ethylmagnesium halide to a mixture of 1 equiv. of carboxylic ester, 1 equiv. of titanium(IV) isopropoxide, and 1.5 equiv. of methylmagnesium halide in ether or tetrahydrofuran at room temperature, has been elaborated. This procedure minimizes the formation of secondary alcohol side products with chromatographic retention factors close to those of the cis-1,2-disubstituted cyclopropanols. Inhibitory action of carboxylic esters toward the reduction of titanium(IV) isopropoxide with Grignard reagents was observed. This observation, along with some other data, allowed us to suggest a modified ate complex mechanism for the cyclopropanation, proceeding via the corresponding octahedral titanium intermediates. In the context of this mechanism, a suitable explanation for the necessity to use an additional equivalent of Grignard reagent in a stoichiometric version of the reaction was found and experimentally verified. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.