358940
6-Heptenoic acid
99%
Synonym(s):
6-Heptanoic acid
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MXP 3,358.00
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MXP 11,462.00
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1 ML
MXP 3,358.00
5 ML
MXP 11,462.00
About This Item
Linear Formula:
CH2=CH(CH2)4COOH
CAS Number:
Molecular Weight:
128.17
Beilstein:
1747265
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
liquid
Assay:
99%
Recommended Products
Quality Level
Assay
99%
form
liquid
refractive index
n20/D 1.439 (lit.)
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
SMILES string
OC(=O)CCCCC=C
InChI
1S/C7H12O2/c1-2-3-4-5-6-7(8)9/h2H,1,3-6H2,(H,8,9)
InChI key
RWNJOXUVHRXHSD-UHFFFAOYSA-N
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General description
Application
6-Heptenoic acid may be used in the preparation of 6-(iodomethyl)-hexanolide, via iodo-lactonization.[3]
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
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)
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