84145-55-1

Basic information

• Product Name: 4-tert-butyl-1-(3,3-dimethoxypropyl)benzene
• Synonyms: 4-tert-butyl-1-(3,3-dimethoxypropyl)benzene;1-(3,3-Dimethoxypropyl)-4-(1,1-dimethylethyl)benzene;1-(4-tert-Butylphenyl)-3,3-dimethoxypropane;Einecs 282-282-7
• CAS NO: 84145-55-1
• Molecular Formula: C₁₅H₂₄O₂
• Molecular Weight: 236.34986
• EINECS: 282-282-7
• Mol File: 84145-55-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 308.8°C at 760 mmHg
• Flash Point: 104°C
• Appearance: /
• Density: 0.939g/cm³
• Vapor Pressure: 0.00121mmHg at 25°C
• Refractive Index: 1.48
• CAS DataBase Reference: 4-tert-butyl-1-(3,3-dimethoxypropyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-tert-butyl-1-(3,3-dimethoxypropyl)benzene(84145-55-1)
• EPA Substance Registry System: 4-tert-butyl-1-(3,3-dimethoxypropyl)benzene(84145-55-1)

Safety Data

• Hazardous Substances Data: 84145-55-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H24O2/c1-15(2,3)13-9-6-12(7-10-13)8-11-14(16-4)17-5/h6-7,9-10,14H,8,11H2,1-5H3

Upstream product

• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 1746-23-2 4-tert-Butylstyrene 

Relevant articles and documents

Selective hydroformylation-acetalization of various olefins using simple and efficient Rh-phosphinite complex catalyst

A simple and efficient Rh-phosphinite complex catalyst was studied for the selective hydroformylation of various olefins. The influence of various reaction parameters including the effect of temperature, pressure, catalyst loading, time, and solvents was studied. The protocol was also applied for the synthesis of various acetals via tandem hydroformylation-acetalization of olefins in alcohols as solvents. High activity and selectivity for acetal formation was achieved in the absence of co-catalysts with admirable substrate to catalyst mole ratio (TON 2500). The developed protocol works for a wide range of olefins to synthesize corresponding aldehydes and acetals under optimized reaction conditions.