Melting point	47-50 ºC
Specific optical rotation	-21 º (c=1%, in MeOH)
Flash point	100 ºC

Symbol(GHS)	Xi
Hazard Codes	R36/37/38
SDS/MSDS	S26;S36

Source	SDS/MSDS Samples
Alfa-Aesar	View & Download
Sigma-Aldrich	View & Download
TCI	View & Download

Synthetic Route

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Articles

Peer-Reviewed Papers

Mutational biosynthesis of a FK506 analogue containing a non-natural starter unit.Yeon Hee Ban et al.Molecular bioSystems, 9(5), 944-947 (2012-12-12) Total synthesis of (.+-.)-methyl shikimate and (.+-.)-3-phosphoshikimic acid. Bartlett PA and McQuaid LA. Journal of the American Chemical Society, 106(25), 7854-7860 (1984) Experimental elicitation with hydroxyisohexyl-3-cyclohexene carboxaldehyde-containing deodorants.Pia Haslund Jørgensen et al.Contact dermatitis, 56(3), 146-150 (2007-02-14) The metabolism of cyclohexanecarboxylic acid and 3-cyclohexenecarboxylic acid by Pseudomonas putida.E R Blakley et al.Canadian journal of microbiology, 28(12), 1324-1329 (1982-12-01) Facilitating the Evolution of Esterase Activity from a Promiscuous Enzyme (Mhg) with Catalytic Functions of Amide Hydrolysis and Carboxylic Acid Perhydrolysis by Engineering the Substrate Entrance Tunnel.Xiaodan Yan et al.Applied and environmental microbiology, 82(22), 6748-6756 (2016-10-30) Synthesis and antiviral evaluation of cis-substituted cyclohexenyl and cyclohexanyl nucleosides.Karine Barral et al.Journal of medicinal chemistry, 48(2), 450-456 (2005-01-22) Comparison of halide impacts on the efficiency of contaminant degradation by sulfate and hydroxyl radical-based advanced oxidation processes (AOPs).Yi Yang et al.Environmental science & technology, 48(4), 2344-2351 (2014-02-01) Bromination of 3-cyclohexene-1-carboxylic acid, epoxydation of methyl 3-cyclohexene-1-carboxylate and opening of methyl cis-and trans-3, 4-epoxycyclohexane-1-carboxylate: Stereochemical results. Bellucci G, et al. Tetrahedron, 28(13), 3393-3399 (1972)

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