4-propylbenzyl bromide
$250.00
CAS No.: 91062-39-4
Catalog No.: 194073
Purity: 95%
MF: C10H13Br
MW: 213.118
Storage: 2-8 degree Celsius
SMILES: C(CC)C1=CC=C(CBr)C=C1
Catalog No.: 194073
Purity: 95%
MF: C10H13Br
MW: 213.118
Storage: 2-8 degree Celsius
SMILES: C(CC)C1=CC=C(CBr)C=C1
4-propylbenzyl bromide; CAS No.: 91062-39-4; 4-propylbenzyl bromide. PROPERTIES: 4-propylbenzyl bromide is a colorless liquid with a molecular formula of C10H13Br, and a molecular weight of approximately 223.12 g/mol. It has a boiling point of around 185-187 C at atmospheric pressure. The compound is moderately soluble in common organic solvents such as ether and chloroform, but is insoluble in water. It should be stored in a tightly sealed, amber glass bottle in a cool, dark place, preferably at temperatures below 10 C. Since it is a bromide compound, it is moisture-sensitive and can hydrolyze in the presence of water. Safety precautions include wearing protective gloves, eye protection, and a lab coat. In case of contact with skin or eyes, immediate flushing with water is required. APPLICATIONS: In organic synthesis, 4-propylbenzyl bromide is a versatile alkylating agent. The benzyl bromide group can react with various nucleophiles such as amines, alcohols, and thiols to form corresponding alkylated products. The propyl substituent on the benzene ring can influence the steric and electronic properties of the resulting compounds. In the preparation of pharmaceutical intermediates, 4-propylbenzyl bromide can be used to introduce benzyl groups into drug molecules to modify their biological activities and pharmacokinetic profiles. For example, in the synthesis of certain antiviral drugs, the benzyl bromide moiety of 4-propylbenzyl bromide can be involved in the construction of the drug's backbone structure, thereby enhancing its antiviral efficacy (as reported in medicinal chemistry journals). Additionally, in the field of chemical research, it can serve as a starting material for the synthesis of novel organic compounds with potential applications in materials science and catalysis (as noted in organic chemistry research papers).
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