6065-71-0

Basic information

• Product Name: 1-Propanol, 2-bromo-, benzoate
• CAS NO: 6065-71-0
• Molecular Formula: C10H11BrO2
• Molecular Weight: 243.1
• Mol File: 6065-71-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Propanol, 2-bromo-, benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanol, 2-bromo-, benzoate(6065-71-0)
• EPA Substance Registry System: 1-Propanol, 2-bromo-, benzoate(6065-71-0)

Safety Data

• Hazardous Substances Data: 6065-71-0(Hazardous Substances Data)

Usage

Uses

intermediate in the synthesis of pharmaceuticals, production of fragrances, flavoring agent

Physical properties

clear, colorless liquid, fruity odor, soluble in alcohol and ether, insoluble in water

Toxicity

low toxicity, but prolonged exposure may cause irritation to the respiratory system and skin

Safety precautions

handle with care and follow proper safety precautions when working with it.

Upstream product

• 37086-84-3 2-hydroxypropyl benzoate 
• 57-55-6 propylene glycol 
• 100-51-6 benzyl alcohol 
• 100-52-7 benzaldehyde 
• 2568-25-4 4-methyl-2-phenyl-1,3-dioxolane 
• 108-86-1 bromobenzene 
• 201230-82-2 carbon monoxide 
• 75-56-9 methyloxirane 

Relevant articles and documents

Ni-Catalyzed Formal Cross-Electrophile Coupling of Alcohols with Aryl Halides

Direct coupling of unactivated alcohols remains a challenge in current synthetic chemistry. We herein demonstrate a strategy building upon in situ halogenation/reductive coupling of alcohols with aryl halides to forge Csp2-Csp3 bonds. The combination of 2-chloro-3-ethylbenzo[d]oxazol-3-ium salt (CEBO) and TBAB as the mild bromination reagents enables rapid transformation of a wide range of alcohols to their bromide counterparts within one to 5 min in CH3CN and DMF, which is compatible with the Ni-catalyzed cross-electrophile coupling conditions in the presence of a chemical reductant. The present method is suitable for arylation of a myriad of structurally complex alcohols with no need for prepreparation of alkyl halides. More importantly, the mild and kinetically rapid bromination process has shown good selectivity in the bromination/arylation of symmetric diols and less sterically hindered hydroxyl groups in polyols, thus offering promise for selective functionalization of diols and polyols without laborious protecting/deprotecting operations. The practicality of this work is also evident in the arylation of a number of carbohydrates, drug compounds, and naturally occurring alcohols.

One-pot synthesis of ω-bromoesters from aromatic aldehydes and diols using pyridinium hydrobromide perbromide

A simple and efficient one-pot procedure has been developed for the synthesis of ω-bromoesters from aromatic aldehydes and diols in the presence of pyridinium hydrobromide perbromide (PHPB) and triethoxymethane in which aldehyde reacts first with diol and the product, cyclic acetal, reacts with PHPB to give the final product, ω-bromoesters.

PALLADIUM COMPLEX-CATALYZED CARBONYLATION OF ORGANIC HALIDES IN THE PRESENCE OF CYCLIC ETHERS: HALOHYDRIN ESTER SYNTHESIS

Cyclic ethers were cleaved by palladium complex-catalyzed carbonylation of organic halides to give halohydrin esters.