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Usage

Uses

Used in Fragrance Industry:
1-(3-Methoxyphenyl)-2-Methylpropan-1-ol is used as a synthetic musk fragrance ingredient for its distinct floral, fruity, and woody scent. It is widely utilized in the production of perfumes, soaps, and other personal care products to enhance their fragrance profiles.
Used in Food and Beverage Industry:
In the food and beverage sector, 1-(3-Methoxyphenyl)-2-Methylpropan-1-ol is used as a flavor ingredient to impart its unique aroma to a variety of products, contributing to the overall sensory experience.
Used in Pharmaceutical Manufacturing:
This chemical compound also finds application in the pharmaceutical industry, where it is employed in the manufacturing process of various medicinal products, likely due to its distinctive properties and potential for interaction with other compounds.
Overall, 1-(3-Methoxyphenyl)-2-Methylpropan-1-ol demonstrates a broad spectrum of applications, showcasing its importance and versatility in different sectors, from personal care and fragrances to the food and pharmaceutical industries.

Upstream product

• 920-39-8 isopropylmagnesium bromide 
• 591-31-1 3-methoxy-benzaldehyde 
• 75-26-3 isopropyl bromide 
• 75-30-9 2-iodo-propane 
• 78-84-2 isobutyraldehyde 

Downstream Products

• 103502-21-2 3-(α-bromo-isobutyl)-anisole 
• 68266-33-1 1-chlor-1-(3'-methoxyphenyl)-2-methyl-propane 
• 102808-14-0 C₂₂H₃₀O₂ 
• 102808-15-1 cis-3,4-bis(3-methoxyphenyl)-2,5-dimethylhex-3-ene 
• 102808-07-1 C₂₀H₂₆O₂ 
• 6026-75-1 1-(3-methoxyphenyl)-2-methyl-propan-1-one 

Relevant academic research and scientific papers

Reaction of secondary and tertiary aliphatic halides with aromatic aldehydes mediated by chromium(II): a selective cross-coupling of alkyl and ketyl radicals

Takai-Utimoto reactions with secondary and tertiary aliphatic halides usually failed according to previous reports. Now, significant improvements could be achieved, and especially secondary aliphatic halides can be coupled to aromatic aldehydes in yields of up to >95%. A variety of processes are competing with the desired one, and thus conditions must be adapted to the nature of the aldehyde as well as the aliphatic halide used, as the outcome of these reactions is strongly affected by the putative radical intermediates.

Influence of Alkyl Chain Ramification on Estradiol Receptor Binding Affinity and Intrinsic Activity of 1,2-Dialkylated 1,2-Bis(4- or 3-hydroxyphenyl)ethane Estrogens and Antiestrogens

The influence of a symmetrical introduction of CH3 substituents in the α or β positions of the 1,2-dialkyl-1,2-bis(4-hydroxyphenyl)ethene estrogens hexestrol (ethyl, HES) and octestrol (n-propyl, OCES) isopropyl (1), tert-butyl (2), sec-butyl (3), isobut

Novel di-(3'-hydroxyphenyl)-alkane compounds, process of preparation and their use in medicine

Compounds of di-(3'-hydroxyphenyl)-alkanes and their methyl ethers, of the formula STR1 wherein R is alkyl and R' is H or methyl, have activity against hormone-dependent breast carcinoma.