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vapor density
>1 (vs air)
Quality Level
Assay
97%
form
liquid
impurities
2% cis-isomer
refractive index
n20/D 1.46 (lit.)
bp
123-125 °C/30 mmHg (lit.)
mp
26-28 °C (lit.)
functional group
carboxylic acid
SMILES string
CC\C=C(/C)C(O)=O
InChI
1S/C6H10O2/c1-3-4-5(2)6(7)8/h4H,3H2,1-2H3,(H,7,8)/b5-4+
InChI key
JJYWRQLLQAKNAD-SNAWJCMRSA-N
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General description
Adsorption and desorption of trans-2-methyl-2-pentenoic acid in dichloromethane has been investigated by using in situ attenuated total reflection infrared spectroscopy. Asymmetric hydrogenation of trans-2-methyl-2-pentenoic acid in hexane over two well defined E-40692 and E-5220 Engelhard Pd/Al2O3 catalysts modified with cinchonidine has been studied.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 2
Flash Point(F)
226.4 °F - closed cup
Flash Point(C)
108 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Heterogeneous asymmetric hydrogenation and deuteration of 2-methyl-2-pentenoic acid over Pd supported catalysts: proton/deuterium exchange.
J. Mol. Catal. A: Chem., 195(1), 181-188 (2003)
Physical chemistry chemical physics : PCCP, 13(43), 19573-19579 (2011-10-06)
Adsorption and desorption of trans-2-methyl-2-pentenoic acid (MPeA) in dichloromethane (CH(2)Cl(2)) were investigated by using in situ attenuated total reflection infrared (ATR-IR) spectroscopy. A liquid flow-through spectroscopic cell allowed for high quality spectra to be obtained from deposited thin films of
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