598-19-6

Basic information

• Product Name: 2-BROMOALLYL ALCOHOL
• Synonyms: 2-BROMOALLYL ALCOHOL;2-Bromo-2-propene-1-ol;2-Bromo-1-propen-3-ol;2-BroMo-2-propylene-1-ol;2-Bromoallyl alcohol 97%
• CAS NO: 598-19-6
• Molecular Formula: C₃H₅BrO
• Molecular Weight: 136.9752
• Product Categories: AcyclicOxygen Compounds;Alcohols;Alkanes;C2 to C6;Organic Building Blocks;Acyclic;Building Blocks;C2 to C6;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
• Mol File: 598-19-6.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 58-62 °C/100 mbar
• Flash Point: 77 °C
• Appearance: /
• Density: 1.654 g/mL at 25 °C
• Vapor Pressure: 0.82mmHg at 25°C
• Refractive Index: n20/D 1.5037
• PKA: 14.35±0.10(Predicted)
• CAS DataBase Reference: 2-BROMOALLYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMOALLYL ALCOHOL(598-19-6)
• EPA Substance Registry System: 2-BROMOALLYL ALCOHOL(598-19-6)

Safety Data

• Hazard Codes: Xn
• Statements: 22-37/38-41
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• Hazardous Substances Data: 598-19-6(Hazardous Substances Data)

Usage

General Description

2-Bromoallyl alcohol is a chemical compound with the molecular formula C3H5BrO. It is a colorless liquid with a strong, unpleasant odor. 2-Bromoallyl alcohol is mainly used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials. It is also used as a reagent in organic chemistry reactions, such as the formation of carbon-carbon bonds. Additionally, it can be used as a solvent in various chemical processes. However, it is important to handle 2-Bromoallyl alcohol with care, as it is toxic and can cause irritation to the skin, eyes, and respiratory system.

InChI:InChI=1/C3H5BrO/c1-3(4)2-5/h5H,1-2H2

Upstream product

• 16400-63-8 2-bromo-3-chloro-propene 
• 513-31-5 2-bromoallyl bromide 
• 107-19-7 propargyl alcohol 
• 63915-88-8 1-acetoxy-2-bromo-2-propene 
• 609-02-9 methyl-malonic acid dimethylester 
• 171922-00-2 2-bromoallyl ethyl carbonate 
• 96-13-9 2,3-Dibromopropan-1-ol 

Downstream Products

• 107-19-7 propargyl alcohol 
• 74886-05-8 bis-(2-bromo-allyl)-ether 
• 56030-46-7 2-(1'-Hydroxycyclohexyl)allylalkohol 
• 56030-48-9 2-methylene-1-phenylpropane-1,3-diol 
• 106202-75-9 2-Bromoprop-2-enyl cyclohex-2-enyl ether 
• 141632-06-6 (3RS,4S)-3-hydroxy-2-hydroxymethyl-6-methyl-4-tritylamino-1,6-heptadiene 
• 116608-28-7 2-(2-bromoprop-2-enyloxy)cyclohexan-1-ol 
• 147298-36-0 1-(((2-bromoallyl)oxy)methyl)-4-methoxybenzene 
• 190067-87-9 2-(3-benzyloxymethyl-3-hydroxy-4-hydroxymethylpent-4-enyl)-2-methyl-1,3-dioxolane 
• 234436-57-8 (S_S)-(+)-2-(p-Tolylsulfinyl)prop-2-en-1-ol 
• 16400-63-8 2-bromo-3-chloro-propene 
• 214753-16-9 (3RS,4S)-4-benzyloxycarbonylamino-3-hydroxy-2-hydroxymethyl-6-methyl-1-heptene 
• 330817-14-6 (3R,4S)-6-Methyl-2-methylene-4-(trityl-amino)-heptane-1,3-diol 
• 330817-15-7 (3S,4S)-6-Methyl-2-methylene-4-(trityl-amino)-heptane-1,3-diol 

Relevant articles and documents

Mechanistic studies of 1-aminocyclopropane-1-carboxylate deaminase: Unique covalent catalysis by coenzyme B6

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BROMINATED FLAME RETARDANTS AND POLYURETHANES CONTAINING THE SAME

The disclosure includes brominated alkenyl alcohols, their use as a flame retardant in polyurethane and polyurethane foams, and polyurethanes containing the brominated alkenyl alcohols. Compositions, methods, and processes are disclosed. The brominated alkenyl alcohols used as flame retardants in polyurethanes can be generally described by Formula (I), the scope of which is disclosed herein.

A simple microwave-assisted preparation of 2-bromo-1-alkenes from 1-alkynes using the LiBr-TMSCl-TEAB reagent system

2-Bromo-1-alkenes are cleanly and conveniently generated in good yields and selectivities via microwave-assisted hydrobromination of 1-alkynes using a combination of lithium bromide (LiBr), chlorotrimethylsilane (TMSCl), and tetraethylammonium bromide (TEAB) in acetonitrile (MeCN).