trans-Hex-2-enoic acid
trans-Hex-2-enoic acid structure
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Common Name | trans-Hex-2-enoic acid | ||
|---|---|---|---|---|
| CAS Number | 13419-69-7 | Molecular Weight | 114.142 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 216.5±0.0 °C at 760 mmHg | |
| Molecular Formula | C6H10O2 | Melting Point | 33-35 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 115.4±9.6 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Mosquito odorant receptor for DEET and methyl jasmonate.
Proc. Natl. Acad. Sci. U. S. A. 111(46) , 16592-7, (2014) Insect repellents are important prophylactic tools for travelers and populations living in endemic areas of malaria, dengue, encephalitis, and other vector-borne diseases. DEET (N,N-diethyl-3-methylbenzamide) is a 6-decade-old synthetic repellent, which is st... |
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Rhodium-catalyzed asymmetric 1, 4-addition of arylboron reagents to α,β-unsaturated esters. Takaya Y, et al.
Tetrahedron Asymmetry 10(20) , 4047-56, (1999)
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Biooxidation of primary alcohols to aldehydes through hydrogen transfer employing janibacter terrae. Orbegozo T, et al.
European J. Org. Chem. 2010(18) , 3445-48, (2010)
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Catalytic residues are shared between two pseudosubunits of the dehydratase domain of the animal fatty acid synthase.
Chem. Biol. 14(12) , 1377-85, (2007) Expression, characterization, and mutagenesis of a series of N-terminal fragments of an animal fatty acid synthase, containing the beta-ketoacyl synthase, acyl transferase, and dehydratase domains, demonstrate that the dehydratase domain consists of two pseud... |