53596-81-9

Basic information

• Product Name: 8-Bromooctan-1-ol acetate
• Synonyms: 8-Bromooctan-1-ol acetate;8-broMo-1-octanol acetate;8-Bromooctyl acetate
• CAS NO: 53596-81-9
• Molecular Formula: C₁₀H₁₉BrO₂
• Molecular Weight: 251.16066
• Mol File: 53596-81-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 149-159 °C(Press: 15-16 Torr)
• Appearance: /
• Density: 1.194±0.06 g/cm3 (20 ºC 760 Torr)
• CAS DataBase Reference: 8-Bromooctan-1-ol acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 8-Bromooctan-1-ol acetate(53596-81-9)
• EPA Substance Registry System: 8-Bromooctan-1-ol acetate(53596-81-9)

Safety Data

• Hazardous Substances Data: 53596-81-9(Hazardous Substances Data)

Usage

General Description

8-Bromooctan-1-ol acetate is a chemical compound with a molecular formula of C10H19BrO2. This substance appears as a clear, colorless liquid and falls under the category of organobromides and carboxylic acid esters. Likewise, it's considered a derivative of alcohol, specifically 1-octanol, which has been brominated and then esterified with acetic acid. Its primary use has historically been in the field of organic synthesis, as it serves as an intermediate for various chemical reactions. Like most organic compounds, it needs to be handled with caution due to potential reactivity and toxicity.

Upstream product

• 50816-19-8 8-bromooctanol 
• 75-36-5 acetyl chloride 
• 629-41-4 1,8-Octanediol 
• 4163-60-4 β-D-galactose peracetate 
• 604-69-3 β-D-glucose pentaacetate 
• 22352-19-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranosyl acetate 
• 108-24-7 acetic anhydride 

Downstream Products

• 807639-81-2 6-quinazolinol, 4-[[3-[(8-hydroxyoctyl)oxy]phenyl]amino]-7-methoxy- 
• 807639-47-0 1-octanol,8-(4-chloro-2-nitrophenoxy)-,acetate(ester) 
• 1056010-65-1 1-octanol, 8-(3-nitrophenoxy)-, acetate (ester) 
• 807639-76-5 benzaldehyde,4-chloro-2-nitro-, O-[8-(acetyloxy)octyl]oxime 
• 231943-23-0 3-dimethylamino-benzoic acid 8-(5-nitro-indol-1-yl)-octyl ester 
• 77328-78-0 (8-Acetoxyoctyl)-triphenylphosphonium-bromid 

Relevant articles and documents

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Facile synthesis of 3-(ω-acetoxyalkyl)thiophenes and derived copolythiophenes using Rieke zinc

An optimized synthetic protocol toward highly reactive Rieke zinc is applied for the preparation of a series of ω-(2,5-dibromothiophene-3-yl) alkyl acetate monomers and statistical copolythiophenes derived thereof, with 10% of ester-functionalized side chains. The obtained conjugated polymers are attractive electron donor materials for organic solar cells, notably to increase the thermodynamic stability of the bulk heterojunction polymer:fullerene active layer blend, and are fully characterized by a combination of spectroscopic, thermal analysis and electrochemical techniques.

Palladium catalyzed cross-coupling reaction of functional organozinc reagents with (2E,4E)- and (2E,4Z)-5-bromopenta-2,4-dienals: Easy access to functional conjugated dienic aldehydes

Functional zinc reagents can be applied to palladium catalyzed cross-coupling reaction with (2E,4E)- and (2E,4Z)-5-bromopenta-2,4-dienal. The corresponding functional dienic aldehydes were obtained in goods yields. From the (2E,4E) isomer, the (2E,4E) dienals were isolated as single isomer according to a total stereoselective reaction. But, from the (2E,4Z) isomer the coupling reaction has lead to a mixture of (2E,4E) and (2E,4Z) isomers. A mechanism for the loss of stereoselectivity in the last case is proposed.