358940
6-Heptenoic acid
99%
Synonym(s):
6-Heptanoic acid
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About This Item
Linear Formula:
CH2=CH(CH2)4COOH
CAS Number:
Molecular Weight:
128.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-283-5
Beilstein/REAXYS Number:
1747265
MDL number:
Assay:
99%
Form:
liquid
InChI key
RWNJOXUVHRXHSD-UHFFFAOYSA-N
InChI
1S/C7H12O2/c1-2-3-4-5-6-7(8)9/h2H,1,3-6H2,(H,8,9)
SMILES string
OC(=O)CCCCC=C
assay
99%
form
liquid
Quality Level
bp
222-224 °C (lit.)
mp
−6.5 °C (lit.)
density
0.946 g/mL at 25 °C (lit.)
functional group
allyl, carboxylic acid
storage temp.
2-8°C
Related Categories
General description
6-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.
Application
6-Heptenoic acid may be used in the preparation of 6-(iodomethyl)-hexanolide, via iodo-lactonization.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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1, 2, 6-Tribromohexane, 5-Hexenylmagnesium Bromide, and 6-Heptenoic Acid1.
Lamb RC and Ayers PW.
The Journal of Organic Chemistry, 27(4), 1441-1442 (1962)
Electrochemical oxidation of adsorbed alkenoic acids as a function of chain length at Pt (111) electrodes. Studies by cyclic voltammetry, EELS and Auger spectroscopy.
Batina N, et al.
Catalysis Letters, 3(4), 275-297 (1989)
Preparation of seven-membered and medium-ring lactones by iodo lactonization.
Simonot B and Rousseau G.
The Journal of Organic Chemistry, 58(1), 4-5 (1993)
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