VINYLACETIC ACID

VINYLACETIC ACID
  • CAS No.:625-38-7
Other grades of this product :
VINYLACETIC ACID Basic information
Product Name:VINYLACETIC ACID
Synonyms:Acetic acid, ethenyl-;Aceticacid,ethenyl-;beta-Butenoic acid;but-3-enoicacid;CH2=CHCH2COOH;Propene-3-carboxylicacid;Vinylessigsαure;Iodoquinol Impurity 4
CAS:625-38-7
MF:C4H6O2
MW:86.09
EINECS:210-892-5
Product Categories:Carbonyl Compounds;Carboxylic Acids;Building Blocks;C1 to C5;Chemical Synthesis;Organic Building Blocks;omega-Functional Alkanols, Carboxylic Acids, Amines & Halides;omega-Unsaturated Carboxylic Acids
Mol File:625-38-7.mol
VINYLACETIC ACID Chemical Properties
Melting point −39 °C(lit.)
Boiling point 163 °C(lit.)
density 1.013 g/mL at 25 °C(lit.)
refractive index n20/D 1.423(lit.)
Fp 150 °F
storage temp. 2-8°C
solubility Fully miscible.
pka4.34(at 25℃)
form Liquid
color Clear colorless to yellow
BRN 1699159
CAS DataBase Reference625-38-7(CAS DataBase Reference)
Safety Information
Hazard Codes C
Risk Statements 22-34-68-43-40
Safety Statements 26-36/37/39-45
RIDADR UN 2922 8/PG 2
WGK Germany 2
HazardClass 8
PackingGroup II
HS Code 29161900
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
VINYLACETIC ACID Usage And Synthesis
Chemical Propertiesclear colourless to yellow liquid
UsesVinylacetic acid used in the preparation of strained nitroso Diels-Aldrer adducts which undergo a domino ROC metathesis in the presence of Ru-carbene catalysts and olefins. It is used in the synthesis of polyethylene glycolated boltorn coatings. It was used to study the inhibition of the enzyme-catalyzed conversion of D-tyrosyl- phenylalanyl-glycine to D-tyrosyl-phenylaline amide by non-peptide carboxylic acids.
Uses3-Butenoic acid was used in the synthesis of polyethylene glycolated boltorn coatings. It was used to study the inhibition of the enzyme-catalysed conversion of D-tyrosyl- phenylalanyl-glycine to D-tyrosyl-phenylaline amide by non-peptide carboxylic acids. It was used in preparation of strained nitroso Diels-Aldrer adducts which undergo a domino ROC metathesis in the presence of Ru-carbene catalysts and olefins.
DefinitionChEBI: That isomer of butenoic acid having the double bond at position C-3.

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