213971-42-7

Usage

Uses

Used in Perfumery Industry:
2,3-DiMethoxy-7-Methyl-6-(phenylMethyl)-1-propylnaphthalene is used as a fragrance additive for its ability to impart a warm and sensual aroma to perfumes. Its long-lasting and intense scent profile is highly valued in creating complex and sophisticated fragrances, contributing to the distinctiveness and appeal of high-end and luxury perfume products.
Despite its significant use in the perfume industry, muscone has also raised environmental and health concerns due to its persistence in the environment and potential toxicity. As a result, there is an ongoing discussion about the need for sustainable alternatives and responsible use of such synthetic compounds in consumer products.

Upstream product

• 142601-49-8 1-bromo-3,4-dimethoxy-2-propylbenzene 
• 215171-91-8 6,7-Dimethoxy-2-methyl-8-propyl-1,2-dihydro-naphthalene 
• 213971-39-2 6-bromo-2,3-dimethoxy-7-methyl-1-propylnaphthalene 
• 215171-97-4 3-Bromo-6,7-dimethoxy-2-methyl-8-propyl-1,2-dihydro-naphthalene 
• 213971-37-0 3,4-dihydro-6,7-dimethoxy-3-methyl-5-n-propyl-1(2H)naphthalenone 
• 213971-36-9 4-[3,4-Dimethoxy-2-n-propylphenyl]-3-methylbutanoicAcid 
• 213971-55-2 (E)-4-(3,4-Dimethoxy-2-propyl-phenyl)-4-hydroxy-3-methyl-but-2-enoic acid 
• 213971-54-1 (E)-4-(3,4-Dimethoxy-2-propyl-phenyl)-4-hydroxy-3-methyl-but-2-enoic acid ethyl ester 
• 74-88-4 methyl iodide 
• 1353852-51-3 1,2-dihydro-6,7-dimethoxy-3-(phenylmethyl)-2-methyl-8-propylnaphthalene 
• 1353852-29-5 2-benzyl-6,7-dimethoxy-3-methyl-5-propyltetralone 
• 1353852-09-1 (E)-2-(benzylidene)-6,7-dimethoxy-3-methyl-5-propyl-1-tetralone 

Downstream Products

• 213971-67-6 7-Benzyl-2,3-dimethoxy-6-methyl-4-propyl-naphthalene-1-carbaldehyde 
• 213971-47-2 7-Benzyl-2,3-dimethoxy-6-methyl-4-n-propyl-1-naphthoic acid 

Relevant academic research and scientific papers

Synthesis of benzyl substituted naphthalenes from benzylidene tetralones

A convenient and efficient synthesis of novel highly substituted dimethoxybenzylnaphthalenes, which are precursors to several dihydroxynaphthoic acids, is described. The approach involves the use of aldol chemistry to provide a number of benzylidene tetra

Hydroxynaphthoic acids and derivatives

In one embodiment, the present invention provides a compound comprising: wherein A=H or OH X=OH, a halogen, OR, NHR, NR'R'' where R, R', and R''=H, C1-8 alkyl, C2-8 alkenyl, or C2-8 alkynyl, cycloalkyl, cycloalkenyl, aryl, aralkyl or heterocyclic, substit

Selective inhibitors of human lactate dehydrogenases and lactate dehydrogenase from the malarial parasite Plasmodium falciparum

Derivatives of the sesquiterpene 8-deoxyhemigossylic acid (2,3- dihydroxy-6-methyl-4-(1-methylethyl)-1-naphthoic acid) were synthesized that contained altered alkyl groups in the 4-position and contained alkyl or aralkyl groups in the 7-position. These su