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About This Item
Linear Formula:
H2C=CH(CH2)3CO2H
CAS Number:
Molecular Weight:
114.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
Quality Level
assay
98%
refractive index
n20/D 1.435 (lit.)
bp
105 °C/15 mmHg (lit.)
density
0.961 g/mL at 25 °C (lit.)
functional group
allyl, carboxylic acid
SMILES string
OC(=O)CCCC=C
InChI
1S/C6H10O2/c1-2-3-4-5-6(7)8/h2H,1,3-5H2,(H,7,8)
InChI key
XUDOZULIAWNMIU-UHFFFAOYSA-N
Application
5-Hexenoic acid may be used for the preparation of iodolactone derivatives and fluorine-containing δ-valerolactones.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
219.2 °F - closed cup
flash_point_c
104 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Synthesis of fluoroalkyl-d-lactones from polyfluoroalkyl iodides and 5-hexenoic acids.
Fang X, et al.
Journal of Fluorine Chemistry, 129(4), 280-285 (2008)
Stilianos G Roussis et al.
Journal of chromatography. A, 1594, 105-111 (2019-03-02)
In an effort to improve separation of impurities in oligonucleotide drugs, alkyl amines of different length and carbon content were evaluated as reagents in ion pair-reversed phase (IP-RP) HPLC with mass spectrometric detection. A range of columns was tested in
Tertiary aminourea-catalyzed enantioselective iodolactonization.
Gemma E Veitch et al.
Angewandte Chemie (International ed. in English), 49(40), 7332-7335 (2010-08-31)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 464929-1G | 04061832356716 |
| 464929-5G | 04061832356730 |
