57825-30-6

Basic information

• Product Name: 1-(bromomethyl)-4-ethylbenzene
• Synonyms: 1-(bromomethyl)-4-ethylbenzene;4-ethylbenzyl bromide（WS204981）
• CAS NO: 57825-30-6
• Molecular Formula: C₉H₁₁Br
• Molecular Weight: 199.09
• Mol File: 57825-30-6.mol
• Article Data: 11

Chemical Properties

• Melting Point: 14.5-15.2 °C
• Boiling Point: 84 °C
• Appearance: /
• Density: 1.312±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 1-(bromomethyl)-4-ethylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(bromomethyl)-4-ethylbenzene(57825-30-6)
• EPA Substance Registry System: 1-(bromomethyl)-4-ethylbenzene(57825-30-6)

Safety Data

• Hazardous Substances Data: 57825-30-6(Hazardous Substances Data)

Usage

General Description

1-(bromomethyl)-4-ethylbenzene is a chemical compound with the formula C9H11Br. It is a derivative of benzene, with a bromomethyl group and an ethyl group attached to the benzene ring. The presence of the bromine atom makes this compound highly reactive, and it is often used as an intermediate in the synthesis of other organic compounds. It is commonly used in organic chemistry research and industrial processes, such as in the production of pharmaceuticals, agrochemicals, and dyes. The compound's structure and properties make it a valuable building block for the creation of new molecules with diverse applications in the chemical industry.

Upstream product

• 50-00-0 formaldehyd 
• 100-41-4 ethylbenzene 
• 10035-10-6 hydrogen bromide 
• 619-64-7 p-ethylbenzoic acid 
• 768-59-2 4-ethylbenzyl alcohol 
• 40391-19-3 (1R*,1'RS*)-1-cyclohex-2-enylethanol 
• 16331-45-6 p-ethylbenzoyl chloride 
• 4748-78-1 4-ethylbenzylaldehyde 
• 1467-05-6 4-ethylbenzylchloride 

Downstream Products

• 1026438-70-9 2-(4-Ethyl-benzyl)-4,4,4-trifluoro-3-oxo-butyric acid ethyl ester 
• 244088-47-9 7-O-p-ethylbenzyl-25-O-methyl-26-O-t-butyldimethylsilylmonensin methyl ester 
• 143251-68-7 2-acetylamino-2-(4-ethylbenzyl)malonic acid diethyl ester 
• 55190-52-8 (4-ethylbenzyl)phosphonic acid diethyl ester 
• 64740-36-9 3-(4-ethyl-phenyl)-propionic acid 
• 351015-27-5 4-ethylbenzylmalonic acid 
• 351014-45-4 vinyl 3-(4-ethylphenyl)propanoate 
• 1025880-82-3 1-benzyl-4-(4-ethyl-benzylidene)-piperidine 
• 193357-73-2 4-(4-ethylbenzyl)piperidine hydrochloride 
• 1427308-25-5 tert-butyl 2,2-dimethyl-5-(4-(4-ethylbenzyl)phenethyl)-1,3-dioxan-5-ylcarbamate 
• 1616633-27-2 methyl 2-(4-bromophenyl)-3-(4-ethylphenyl)propanoate 
• 660842-01-3 1,3-dimethoxy-2-(4-ethylbenzyl)benzene 
• 1148137-40-9 1-(1H-1,2,4-triazol-1-yl)-2-(2,4-difluorophenyl)-3-[N-butyl-N-(4-ethylbenzyl)amino]-2-propanol 

Relevant articles and documents

Tandem catalytic C(sp3)-H amination/sila-sonogashira-hagihara coupling reactions with iodine reagents

A new tandem C-N and C-C bond-forming reaction has been achieved through RhII/Pd0 catalysis. The sequence first involves an iodine(III) oxidant, then the in situ generated iodine(I) by-product is used as a coupling partner. The overall process demonstrates the synthetic value of iodoarenes produced in trivalent iodine reagent mediated oxidations. I(003) is a double agent: A tandem C-N and C-C bond-forming reaction has been achieved through RhII/Pd0 catalysis. The sequence first involves an iodine(III) oxidant, then the in situ generated iodine(I) by-product is used as a coupling partner. The overall process affords complex building blocks with high yields, and demonstrates the synthetic value of iodoarenes produced in trivalent iodine reagent mediated oxidations.

Process for Producing Aromatic Aldehyde Compound

A process for producing an aromatic aldehyde compound has steps of converting alkyl-substituted or non-substituted benzene into a compound of formula I by halomethylation, and allowing the compound of formula I and alkyl aldehyde to react in presence of phase transfer catalyst at a reaction temperature under alkaline condition to obtain the aromatic aldehyde compound.

Making a difference on excited-state chemistry by controlling free space within a nanocapsule: Photochemistry of 1-(4-alkylphenyl)-3-phenylpropan-2-ones

The free space within a reaction cavity plays a determining role during the excited-state reaction of 1-(4-alkylphenyl)-3-phenylpropan-2-ones included within a capsule formed by two molecules of a deep cavity cavitand. By controlling the free space within the reaction cavity through remote alkyl substitution on the reactant ketone it is possible to control the yield of the rearrangement product shown above.