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线性分子式:
CH3(CH2)3CH(C2H5)CO2H
化学文摘社编号:
分子量:
144.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-743-6
Beilstein/REAXYS Number:
1750468
MDL number:
Assay:
99%
Form:
liquid
InChI key
OBETXYAYXDNJHR-UHFFFAOYSA-N
InChI
1S/C8H16O2/c1-3-5-6-7(4-2)8(9)10/h7H,3-6H2,1-2H3,(H,9,10)
SMILES string
CCCCC(CC)C(O)=O
vapor density
4.98 (vs air)
vapor pressure
<0.01 mmHg ( 20 °C), 10 mmHg ( 115 °C)
assay
99%
form
liquid
autoignition temp.
699 °F
expl. lim.
1.04 %, 135 °F, 8.64 %, 188 °F
Quality Level
bp
228 °C (lit.)
density
0.903 g/mL at 25 °C (lit.)
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Application
2-Ethylhexanoic acid can be used:
- As a reactant in esterification , decarboxylative alkynylation , and preparation of alkyl coumarins via decarboxylative coupling reactions.
- In the organocatalytic medium for the preparation of various 3,4-dihydropyrimidin-2(1H)-ones/thiones by Biginelli reaction.
signalword
Danger
hcodes
Hazard Classifications
Repr. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
237.2 °F - closed cup
flash_point_c
114 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Esterification of aliphatic acids with olefin promoted by Bronsted acidic ionic liquids
Gu Y, et al.
J. Mol. Catal. A: Chem., 212(1-2), 71-75 (2004)
Novel and efficient organocatalytic biginelli reaction using 2-ethylhexanoic acid
Hekmatshoar R, et al.
Gazi University Journal of Science, 25(3), 617-621 (2012)
Direct C-3 alkylation of coumarins via decarboxylative coupling with carboxylic acids
Jafarpour F, et al.
New. J. Chem., 43(24), 9328-9332 (2019)
Silver-catalyzed decarboxylative alkynylation of aliphatic carboxylic acids in aqueous solution
Liu X, et al.
Journal of the American Chemical Society, 134(35), 14330-14333 (2012)
Iron (III)-catalyzed direct synthesis of diphenylmethyl esters from 2-diphenylmethoxypyridine
Tran Van H, et al.
Synthetic Communications, 212(1-2), 1-9 (2019)
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