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6-Heptenoic acid

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CAS:1119-60-4
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CAS:1119-60-4
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CAS:1119-60-4
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CAS:1119-60-4
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  • 6-HEPTENOIC ACID
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  • 2024-03-28
  • CAS:1119-60-4
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6-Heptenoic acid Basic information
Product Name:6-Heptenoic acid
Synonyms:RARECHEM AL BO 1361;6-HEPTENOIC ACID;hept-6-enoic acid;6-Heptenoic acid 99%;Hept-6-enoicaci;Hept-6-enoic acid,97%(stabilized with MEHQ)
CAS:1119-60-4
MF:C7H12O2
MW:128.17
EINECS:214-283-5
Product Categories:C7;Carbonyl Compounds;Carboxylic Acids;Building Blocks;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks
Mol File:1119-60-4.mol
6-Heptenoic acid Structure
6-Heptenoic acid Chemical Properties
Melting point -6.5 °C (lit.)
Boiling point 222-224 °C (lit.)
density 0.946 g/mL at 25 °C (lit.)
refractive index n20/D 1.439(lit.)
Fp >230 °F
storage temp. 2-8°C
form liquid
pka4.75±0.10(Predicted)
color Colourless to light yellow
Water Solubility Miscible with water.
BRN 1747265
InChIInChI=1S/C7H12O2/c1-2-3-4-5-6-7(8)9/h2H,1,3-6H2,(H,8,9)
InChIKeyRWNJOXUVHRXHSD-UHFFFAOYSA-N
SMILESC(O)(=O)CCCCC=C
LogP1.930 (est)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR UN 3265 8/PG 3
WGK Germany 3
HazardClass 8
PackingGroup II
HS Code 2916199590
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
6-Heptenoic acid Usage And Synthesis
Uses6-Heptenoic acid may be used in the preparation of 6-(iodomethyl)-hexanolide, via iodo-lactonization.
DefinitionChEBI: 6-Heptenoic acid is a heptenoic acid with the double bond at position 6.
Synthesis Reference(s)Journal of the American Chemical Society, 107, p. 4230, 1985 DOI: 10.1021/ja00300a025
Tetrahedron, 51, p. 4991, 1995 DOI: 10.1016/0040-4020(95)98696-F
Tetrahedron Letters, 24, p. 4439, 1983
General Description6-Heptenoic acid is a straight-chain terminal alkenoic acid. Electrochemical oxidation of 6-heptenoic acid adsorbed on Pt(111) electrode surface has been reported. Preparation of 6-heptenoic acid has been reported.
Synthesissynthesis of 6-Heptenoic acid and higher homologs of this ω-unsaturated acid, a study of the pyrolysis of wheptano lactone was undertaken. The lactone was prepared by the oxidation of cycloheptanone under Baeyer-Villiger conditions. The pyrolysis of ω-unsaturated acid was effected by dropping the substance under a nitrogen atmosphere into a heated column packed with glass beads.
Synthesis of 6-Heptenoic Acid
PrecautionsIncompatible with strong oxidizing agents, strong acids and bases.
Tag:6-Heptenoic acid(1119-60-4) Related Product Information
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