Identification | Back Directory | [Name]
(1alpha,2beta,4beta)-1-methyl-2,4-bis(methylvinyl)-1-vinylcyclohexane | [CAS]
33880-83-0 | [Synonyms]
Elemene (-)-β-elemene Elemene - mixture of isomers 1-Ethenyl-1-methyl-2,4-di(prop-1-en-2-yl)cyclohexane (1R,2R,4S)-1-Methyl-1-vinyl-2,4-diisopropenylcyclohexane [1R,(+)]-1-Methyl-2β,4β-diisopropenyl-1-vinylcyclohexane 1α-Ethenyl-1-methyl-2β,4β-bis(1-methylethenyl)cyclohexane (1alpha,2beta,4beta)-1-methyl-2,4-bis(methylvinyl)-1-vinylcyclohexane Cyclohexane,1-ethenyl-1-Methyl-2,4-bis(1-Methylethenyl)-, (1R,2R,4S)-rel- 2-((1R,3S,4S)-4-methyl-3-(prop-1-en-2-yl)-4-vinylcyclohexyl)prop-2-en-1-ol (1alpha,2beta,4beta)-1-methyl-2,4-bis(methylvinyl)-1-vinylcyclohexane USP/EP/BP β-elemene,(1alpha,2beta,4beta)-1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-cyclohexane,β-elemene | [EINECS(EC#)]
251-713-0 | [Molecular Formula]
C15H24 | [MOL File]
33880-83-0.mol | [Molecular Weight]
204.351 |
Chemical Properties | Back Directory | [Boiling point ]
277.87°C (rough estimate) | [density ]
0.8749 | [refractive index ]
1.4935 | [Odor]
at 100.00 %. herbal waxy fresh | [Odor Type]
herbal | [InChI]
InChI=1/C15H24/c1-7-15(6)9-8-13(11(2)3)10-14(15)12(4)5/h7,13-14H,1-2,4,8-10H2,3,5-6H3/t13-,14+,15-/s3 | [InChIKey]
OPFTUNCRGUEPRZ-XUPSQSTFNA-N | [SMILES]
[C@]1(C=C)(C)CC[C@H](C(C)=C)C[C@@H]1C(C)=C |&1:0,6,11,r| | [LogP]
5.772 (est) | [EPA Substance Registry System]
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis( 1-methylethenyl)-, (1R,2R,4S)-rel-(33880-83-0) |
Hazard Information | Back Directory | [Uses]
β-Elemene is an active constituent of Delonix regia and an anti-inflammatory agent. β-Elemene is a useful compound for investigating the toll-like receptor 4 signaling pathway and the inhibition of TNF-?a, IL-?1b, IL-?6 and IL-?12 expressions. | [Definition]
ChEBI: (-)-beta-elemene is the (-)-enantiomer of beta-elemene that has (1S,2S,4R)-configuration. It has a role as an antineoplastic agent. | [Anticancer Research]
For this compound, a reduction of tumoral cell proliferation in human and murinemodels was reported (Misharina et al. 2013). |
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BOC Sciences
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https://www.bocsci.com |
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