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Usage

Uses

Used in Research Laboratories:
1-(bromoMethyl)-4-heptyl-benzene is used as a chemical intermediate for the synthesis of other organic compounds, contributing to the advancement of chemical research and development.
Used in Industrial Settings:
In the industrial sector, 1-(bromoMethyl)-4-heptyl-benzene is employed as a building block for creating a range of organic compounds, which can be further utilized in various applications such as pharmaceuticals, agrochemicals, and materials science.

Upstream product

• 171627-60-4 4-heptylbenzyl alcohol 
• 623-24-5 1,4-bis(bromomethyl)benzene 
• 111-25-1 1-bromo-hexane 
• 3761-92-0 n-hexylmagnesium bromide 
• 861906-61-8 4-heptylbenzyl diphenylphosphinate 

Downstream Products

• 121679-98-9 2-Heptyl-5-[4-(4-heptyl-benzyloxy)-phenyl]-[1,3,4]thiadiazole 
• 407619-25-4 4-n-heptylphenylmethanethiol 
• 407619-28-7 (2R,5R)-2-[1-(4-Heptyl-benzylsulfanyl)-1-methyl-ethyl]-5-methyl-cyclohexanone 
• 1342883-91-3 4-{3-[4-(4-n-heptylbenzyloxy)phenyl]-1,2,4-oxadiazol-5-yl}phenyl 4-hexylbenzoate 
• 1427308-30-2 tert-butyl 2,2-dimethyl-5-(4-(4-heptylbenzyl)phenethyl)-1,3-dioxan-5-ylcarbamate 
• 1613754-07-6 C₄₂H₅₀N₂O₃ 

Relevant academic research and scientific papers

Trimethylsilyl triflate mediated new carbon-carbon bond forming reactions between benzyl diphenylphosphinates and organosilicon compounds

The trimethylsilyl triflate mediated reaction of benzyl diphenylphosphinate with allyltrimethylsilane or trimethylsilyl enolate afforded the corresponding cross-coupling products in good yields. Copyright

Development of Odorless Thiols and Sulfides and Their Applications to Organic Synthesis

Development of new odorless thiols (dodecanethiol, 4-n- heptylphenylmethanethiol, 4-trimethylsilylphenylmethanethiol, 4-trimethylsilylbenzenethiol) and an odorless sulfide (1-methylsulfanyldodecane) and their applications to dealkylation, Michael addition, Swern oxidation, and Corey-Kim oxidation are described.

Odorless substitutes for foul-smelling thiols: Syntheses and applications

Several alkanethiols and p-alkylphenylmethanethiols were synthesized, and their odors were compared with those of ethanethiol and benzyl mercaptan by human and instrumental sensors. Among the various thiols analyzed, 1-dodecanethiol (1) and p-heptylphenylmethanethiol (3) were revealed to be odorless. 1-Dodecanethiol (1) has been used instead of ethanethiol for dealkylation of ethers, and p-heptylphenylmethanethiol (3) can replace benzyl mercaptan in the preparation of a 1,3-mercapto alcohol from an α,β-unsaturated ketone. These odorless thiols will greatly improve the physical environment of the researcher working with these foul-smelling compounds.