d-Carvone

Base Information Edit

Chemical Name:d-Carvone
CAS No.:2244-16-8
Deprecated CAS:53763-73-8
Molecular Formula:C₁₀H₁₄O
Molecular Weight:150.221
Hs Code.:29142900
European Community (EC) Number:218-827-2
UN Number:2810
UNII:4RWC1CMS3X
DSSTox Substance ID:DTXSID8020256
Nikkaji Number:J9.490K
Wikidata:Q27889969
Metabolomics Workbench ID:38529
ChEMBL ID:CHEMBL501949
Mol file:2244-16-8.mol

Synonyms:d-Carvone;2244-16-8;(+)-Carvone;(S)-(+)-Carvone;(S)-Carvone;(S)-2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-enone;D(+)-Carvone;(+)-(S)-Carvone;Carvone, (+)-;D-(+)-Carvone;(S)-(+)-p-Mentha-6,8-dien-2-one;S-(+)-carvone;Carvol;d-Carvone (natural);(+)-(4S)-carvone;(5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one;p-Mentha-6,8-dien-2-one, (S)-(+)-;2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (5S)-;CCRIS 2385;d-1-Methyl-4-isopropenyl-6-cyclohexen-2-one;Talent;CHEBI:15399;UNII-4RWC1CMS3X;2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (S)-;4RWC1CMS3X;(S)-d-p-Mentha-6,8,(9)-dien-2-one;(S)-2-Methyl-5-(1-methylvinyl)cyclohex-2-en-1-one;EINECS 218-827-2;d-p-Mentha-6,8,(9)-dien-2-one;(4S)-carvone;DTXSID8020256;AI3-39004;CARVONE D-;CARVONE, D-;DTXCID00256;(5S)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-one;(5S)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-one;(S)-2-methyl-5-(1-methylethenyl)-2-Cyclohexen-1-one;(S)-5-Isopropenyl-2-methyl-2-cyclohexenone;(S)-5-isopropenyl-2-methylcyclohex-2-en-1-one;d-p-Mentha-6,8(9)-dien-2-one;(4S)-p-mentha-1(6),8-dien-2-one;FEMA NO. 2249, (+)-;(5S)-2-methyl-5-(1-methylethenyl)cyclohex-2-en-1-one;MFCD00062997;CAS-2244-16-8;(S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one;dextro-carvone;s-carvone;d-carvon;(+)carvone;5-isopropenyl-2-methylcyclohex-2-en-1-one;S(+)-Carvone;carvone, (S)-isomer;D-CARVOL;CARVONE D-FORM;Epitope ID:141510;CARVONE D-FORM [MI];MLS002415723;SCHEMBL184022;(+)-CARVONE [FCC];D-Carvone, >=96%, FG;2-Methyl-4-(1 -methylethenyl)-2-cyclohexene-1 -one;CHEMBL501949;(5S)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-one;(S)-(+)-Carvone, 96%;(+)-Carvone, analytical standard;HMS3039E10;LS-73;Tox21_201441;Tox21_302743;s6049;AKOS016843871;AM84798;CS-W014295;DS-4662;HY-W013579;6-allyl-4,5-dimethoxy-1,3-benzodioxol;NCGC00091882-01;NCGC00091882-02;NCGC00091882-03;NCGC00091882-04;NCGC00256315-01;NCGC00258992-01;(S)-(+)-p-mentha-6,8-dien- 2-one;SMR001370898;p-Mentha-6,8-dien-2-one, (S)-()-;EN300-393032;O10215;A816212;5-Isopropenyl-2-methyl-2-cyclohexen-1-one, (S)-;Q-200930;Q27889969;Z1255356261;(+)-Carvone, certified reference material, TraceCERT(R);D-Carvone 2-Methyl-5-(1-methylethenyl)-2-cyclohexene-1-one;(S) - 2 - methyl - 5 - (1 - methylvinyl)cyclohex - 2 - en - 1 - one;0WU

Suppliers and Price of d-Carvone

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 117 raw suppliers

Chemical Property of d-Carvone Edit

Chemical Property:

Appearance/Colour:colourless or pale yellow liquid
Vapor Pressure:0.0656mmHg at 25°C
Melting Point:88.9°C
Refractive Index:n20/D 1.499
Boiling Point:230.5 °C at 760 mmHg
Flash Point:88.9 °C
PSA：17.07000
Density:0.94 g/cm³
LogP:2.48790
Water Solubility.:<0.1 g/100 mL at 25℃
XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:150.104465066
Heavy Atom Count:11
Complexity:223
Transport DOT Label:Poison

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Safety Statements: S24/25:;

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CC1=CCC(CC1=O)C(=C)C
Isomeric SMILES:CC1=CC[C@@H](CC1=O)C(=C)C

Technology Process of d-Carvone

There total 114 articles about d-Carvone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: 99-48-9,1197-06-4,1197-07-5,2102-58-1,2102-59-2,5157-78-8,5503-11-7,7632-16-8,18383-51-2,22567-18-6,20307-86-2
(4R,6R)-carveol

: 6485-40-1,2244-16-8
(R)-Carvone

Guidance literature:: With oxygen; tris(triphenylphosphine)ruthenium(II) chloride; In 1,2-dichloro-ethane; under 760 Torr; Ambient temperature;
DOI:10.1039/c39810000907

Reference yield: 89.0%

: 36616-60-1
(1R,4R,6R)-4-isopropenyl-1-methyl-7-oxabicyclo[4.1.0]heptan-2-one

: 6485-40-1,2244-16-8
(R)-Carvone

Guidance literature:: With sodium hydroxide; thiourea dioxide; tetrabutylammomium bromide; In tetrahydrofuran; at 50 ℃; for 0.5h;
DOI:10.1016/S0040-4039(96)02451-3

Reference yield: 79.0%

: 677326-54-4
2,3-epoxy-5-isopropenyl-2-methylcyclohexanone

: 6485-40-1,2244-16-8
(R)-Carvone

Guidance literature:: With hydrogen; triethyl phosphite; In isopropyl alcohol; at 100 ℃; for 32h; under 6000.6 Torr; chemoselective reaction; Glovebox;
DOI:10.1039/d0cy01695k