60982-74-3

Basic information

• Product Name: 1-(broMoMethyl)-4-heptyl-benzene
• Synonyms: 1-(broMoMethyl)-4-heptyl-benzene
• CAS NO: 60982-74-3
• Molecular Formula: C₁₄H₂₁Br
• Molecular Weight: 269.22054
• Mol File: 60982-74-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(broMoMethyl)-4-heptyl-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(broMoMethyl)-4-heptyl-benzene(60982-74-3)
• EPA Substance Registry System: 1-(broMoMethyl)-4-heptyl-benzene(60982-74-3)

Safety Data

• Hazardous Substances Data: 60982-74-3(Hazardous Substances Data)

Usage

Description

1-(bromoMethyl)-4-heptyl-benzene is an organic compound characterized by a benzene ring with a bromomethyl group at the first carbon and a heptyl group at the fourth carbon. It is a colorless liquid with the molecular formula C14H21Br and is utilized in the synthesis of various organic compounds. Due to its hazardous nature, it is crucial to handle this chemical with proper safety measures.

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

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

Downstream Products

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

Relevant articles and documents

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

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.