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Vinyl bromide

Base Information
  • Chemical Name:Vinyl bromide
  • CAS No.:593-60-2
  • Molecular Formula:C2H3Br
  • Molecular Weight:106.95
  • Hs Code.:29033990
  • European Community (EC) Number:209-800-6
  • ICSC Number:0597
  • UN Number:1085
  • UNII:83NRW59KFY
  • DSSTox Substance ID:DTXSID8021432
  • Nikkaji Number:J4.073H
  • Wikipedia:Vinyl_bromide
  • Wikidata:Q421041
  • NCI Thesaurus Code:C44346
  • Metabolomics Workbench ID:57694
  • Mol file:593-60-2.mol
Vinyl bromide

Synonyms:vinyl bromide

Suppliers and Price of Vinyl bromide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Vinyl bromide
  • 2mL
  • $ 60.00
  • TCI Chemical
  • Vinyl Bromide (ca. 12% in Tetrahydrofuran, ca. 1.0mol/L)
  • 100mL
  • $ 91.00
  • SynQuest Laboratories
  • Vinyl bromide 98%
  • 1 kg
  • $ 355.00
  • Sigma-Aldrich
  • Vinyl bromide 98%
  • 100g
  • $ 161.00
  • Sigma-Aldrich
  • Vinyl bromide 98%
  • 900g
  • $ 419.00
  • Sigma-Aldrich
  • Vinyl bromide solution 1.0 M in THF
  • 800ml
  • $ 372.00
  • Sigma-Aldrich
  • Vinyl bromide 98%
  • 2.2kg
  • $ 881.00
  • Sigma-Aldrich
  • Vinyl bromide solution 1.0 M in THF
  • 100ml
  • $ 85.70
  • Oakwood
  • Vinyl bromide
  • 100g
  • $ 40.00
  • Oakwood
  • Vinyl bromide
  • 25g
  • $ 25.00
Total 18 raw suppliers
Chemical Property of Vinyl bromide
Chemical Property:
  • Appearance/Colour:colourless liquid 
  • Vapor Pressure:1551 mm Hg ( 37.8 °C) 
  • Melting Point:-139 °C(lit.) 
  • Refractive Index:n20/D 1.410  
  • Boiling Point:15.799 °C at 760 mmHg 
  • Flash Point:1 °F  
  • PSA:0.00000 
  • Density:1.532 g/cm3 
  • LogP:1.52480 
  • Storage Temp.:2-8°C 
  • Water Solubility.:insoluble 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:105.94181
  • Heavy Atom Count:3
  • Complexity:10.3
  • Transport DOT Label:Flammable Gas
Purity/Quality:

99.9% *data from raw suppliers

Vinyl bromide *data from reagent suppliers

Safty Information:
  • Pictogram(s): ToxicT; HighlyF+ 
  • Hazard Codes:F+,T,F 
  • Statements: 45-12-19-36/37-22-11 
  • Safety Statements: 53-9-16-29-33-45-26 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Plastics & Rubber -> Vinyl Halides
  • Canonical SMILES:C=CBr
  • Inhalation Risk:A harmful concentration of this gas in the air will be reached very quickly on loss of containment.
  • Effects of Short Term Exposure:Rapid evaporation of the liquid may cause frostbite. The substance is irritating to the eyes. The substance may cause effects on the central nervous system.
  • Effects of Long Term Exposure:This substance is probably carcinogenic to humans.
  • Uses Vinyl bromide is used as a fire retardant inplastics. Production of flame-resistant plastics or thermoplastic resins.
Technology Process of Vinyl bromide

There total 53 articles about Vinyl bromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With potassium hydroxide; In ethanol; at 40 ℃; for 1h;
DOI:10.1021/ol200499t
Guidance literature:
With N,N-dimethyl-formamide; potassium bromide; trichlorophosphate; In acetonitrile; at 20 ℃; Reagent/catalyst; Sonication;
DOI:10.1080/15533174.2014.989573
Refernces

First total synthesis of mytiloxanthin

10.1248/cpb.48.1833

The research describes the first total synthesis of mytiloxanthin 2, a compound with a unique cyclopentyl enolic β-diketone group conjugated to the polyene chain. The purpose of this study was to achieve the biomimetic total synthesis of mytiloxanthin 2 using a stereoselective rearrangement of epoxides. Important reagents include p-methoxybenzyloxymethyl (PMBM) chloride for protection, LiAlH? for reduction, o-iodoxybenzoic acid (IBX) for oxidation, and vinyl bromide 13 for the introduction of the C10-unit. The synthesis involved several steps, including the reduction of ketone 7 to obtain compound 11, conversion to aldehyde 12, and subsequent oxidation to yield ketone 14. The final steps involved the protection of the diketone moiety with an acetyl group to form acetate 17, partial deprotection with tetrabutylammonium fluoride (TBAF), oxidation with IBX, and final deprotection with HF to obtain the cis-β-diketone-aldehyde 8b. The cis-aldehyde 8b was then reacted with the C10-phosphonium salt 19 in the presence of KOH to form an isomeric mixture, which was condensed with the acetylenic Wittig salt 20 to yield mytiloxanthin 2. The spectral data of the synthesized mytiloxanthin 2 were in good agreement with those of a natural specimen, confirming the successful total synthesis.

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