(-)-Carvone - CAS 6485-40-1
Catalog: |
BB032573 |
Product Name: |
(-)-Carvone |
CAS: |
6485-40-1 |
Synonyms: |
(R)-(-)-Carvone; l-Carvone |
IUPAC Name: | (5R)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-one |
Description: | (-)-Carvone (CAS# 6485-40-1) is an antinociceptive monoterpene found as the main active constituent of essential oils obtained from plants of the genus Mentha. It is a novel agonist of TRPV1 channels. It can also be used as a chiral starting material. |
Molecular Weight: | 150.22 |
Molecular Formula: | C10H14O |
Canonical SMILES: | CC1=CCC(CC1=O)C(=C)C |
InChI: | InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m1/s1 |
InChI Key: | ULDHMXUKGWMISQ-SECBINFHSA-N |
Boiling Point: | 227-230 °C |
Melting Point: | 25.2°C |
Flash Point: | 88°C |
Purity: | > 95 % |
Density: | 0.958 g/cm3 |
Appearance: | Oil |
Storage: | 2-8°C |
MDL: | MFCD00001578 |
LogP: | 2.48790 |
Refractive Index: | 1.495-1.502 |
Stability: | Stable under normal temperatures and pressures. |
GHS Hazard Statement: | H302 (83.3%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P272, P280, P301+P312, P302+P352, P321, P330, P333+P313, P363, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113151205-A | Alcohol dehydrogenase mutant and application thereof in cyclic terpene ketone synthesis | 20210420 |
CN-113115799-A | Application of turmeric volatile oil | 20210401 |
CN-112956730-A | CBD-containing mint electronic atomized liquid and preparation method thereof | 20210311 |
CN-112898159-A | Ester compound and preparation method and application thereof | 20210129 |
CN-112662639-A | Short-chain alcohol dehydrogenase and application thereof | 20210121 |
PMID | Publication Date | Title | Journal |
31858786 | 20200217 | CRISPR-Generated Nrf2a Loss- and Gain-of-Function Mutants Facilitate Mechanistic Analysis of Chemical Oxidative Stress-Mediated Toxicity in Zebrafish | Chemical research in toxicology |
30662405 | 20180101 | The Potential of Isoprenoids in Adjuvant Cancer Therapy to Reduce Adverse Effects of Statins | Frontiers in pharmacology |
27750016 | 20170417 | Toward the Design of Less Hazardous Chemicals: Exploring Comparative Oxidative Stress in Two Common Animal Models | Chemical research in toxicology |
23094646 | 20121102 | Total synthesis of alotaketal A | Organic letters |
21428701 | 20120901 | Enantioselective penetration enhancing effect of carvone on the in vitro transdermal permeation of nicorandil | Pharmaceutical development and technology |
Complexity: | 223 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 150.104465066 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 150.104465066 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 17.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.4 |
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