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470-67-7 | 1,4-Cineole
CAS No: 470-67-7 Catalog No: AG003DNB MDL No:
Product Description
Catalog Number:
AG003DNB
Chemical Name:
1,4-Cineole
CAS Number:
470-67-7
IUPAC Name:
1-methyl-4-propan-2-yl-7-oxabicyclo[2.2.1]heptane
InChI:
InChI=1S/C10H18O/c1-8(2)10-6-4-9(3,11-10)5-7-10/h8H,4-7H2,1-3H3
InChI Key:
RFFOTVCVTJUTAD-UHFFFAOYSA-N
EC Number:
207-428-9
UNII:
B55JTU839B
FEMA Number:
3658
Properties
Complexity:
164
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
154.136g/mol
Formal Charge:
0
Heavy Atom Count:
11
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
154.253g/mol
Monoisotopic Mass:
154.136g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
9.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.5
Literature
| Title | Journal |
|---|---|
| Interaction of plant essential oil terpenoids with the southern cattle tick tyramine receptor: A potential biopesticide target. | Chemico-biological interactions 20170201 |
| Small molecules inhibit growth, viability and ergosterol biosynthesis in Candida albicans. | SpringerPlus 20130101 |
| Quantitative structure-activity relationships of monoterpenoid binding activities to the housefly GABA receptor. | Pest management science 20120801 |
| Toxicity of Rhododendron anthopogonoides essential oil and its constituent compounds towards Sitophilus zeamais. | Molecules (Basel, Switzerland) 20110825 |
| Interactions between novel terpenes and main components of rat and human skin: mechanistic view for transdermal delivery of propranolol hydrochloride. | Current drug delivery 20110301 |
| Anxiolytic-like effect of the monoterpene 1,4-cineole in mice. | Pharmacology, biochemistry, and behavior 20100901 |
| [Analysis of the chemical constituents of essential oil from Chimonanthus zhejiangensis by GC-MS]. | Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials 20100301 |
| Roles of cytochrome P450 3A enzymes in the 2-hydroxylation of 1,4-cineole, a monoterpene cyclic ether, by rat and human liver microsomes. | Xenobiotica; the fate of foreign compounds in biological systems 20011001 |
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