Merck
Todas as fotos(1)

435759

Sigma-Aldrich

(S)-(+)-Carvone

96%

Todas as fotos(1)
Sinônimo(s):
p-Mentha-6,8-dien-2-one, (+)-Carvone, (S)-5-Isopropenyl-2-methyl-2-cyclohexenone
Empirical Formula (Hill Notation):
C10H14O
Número CAS:
2244-16-8
Peso molecular:
150.22
Beilstein:
2042970
Número EC:
218-827-2
Número MDL:
MFCD00062997
ID de substância PubChem:
24867255
NACRES:
NA.22

Nível de qualidade

100

teor

96%

forma

liquid

atividade óptica

[α]23/D +55.0±7°, neat

índice de refração

n20/D 1.497 (lit.)

pb

96-98 °C/10 mmHg (lit.)

densidade

0.96 g/mL at 25 °C (lit.)

SMILES string

CC(=C)[C@H]1CC=C(C)C(=O)C1

InChI

1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m0/s1

InChI key

ULDHMXUKGWMISQ-VIFPVBQESA-N

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Descrição geral

(S)-(+)-Carvone, a monoterpene found mainly in caraway and dill seed oils, is used in cosmetic, food and pharmaceutical preparations.

Aplicação

(S)-(+)-Carvone can be used as a starting material to synthesize:
  • (-)-Samaderine Y, a pentacyclic quassinoid.
  • (-)-Ambrox, a terpenoid responsible for the odor of ambergris.
  • 3β-Acetoxydrimenin (a sesquiterpene) via conjugated addition of potassium cyanide followed by base catalyzed Robinson annulation reaction.
  • Thapsigargin family members such as trilobolide, nortrilobolide, and thapsivillosin F.

Embalagem

5 mL in glass bottle
25 mL in poly bottle
(S)-(+)-Carvone, a monoterpene found mainly in caraway and dill seed oils, is used in cosmetic, food and pharmaceutical preparations.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H317

Classificações de perigo

Skin Sens. 1A

Código de classe de armazenamento

10 - Combustible liquids

WGK

WGK 1

Ponto de fulgor (ºF)

204.1 °F - closed cup

Ponto de fulgor (ºC)

95.6 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificado de análise

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Certificado de origem

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Mais documentos

FT-IR Condensed Phase
FT-NMR Spectra
Pressure-Temperature Nomograph
Spectra - ATR-IR
Structure Search

Quotes and Ordering

Bulk Quote-Order Product
Total Synthesis of (-)-Samaderine Y from (S)-(+)-Carvone
Shing TKM and Yeung YY
Angewandte Chemie (International Edition in English), 117(48), 8195-8198 (2005)
Total synthesis of (-)-Ambrox from S-(+)-carvone (part 6)
Verstegen-Haaksma AA, et al.
Tetrahedron, 50(33), 10095-10106 (1994)
Are vectors able to learn about their hosts? A case study with Aedes aegypti mosquitoes.
Alonso WJ, et al.
Memorias do Instituto Oswaldo Cruz, 98(5), 665-672 (2003)
Wladimir J Alonso et al.
Memorias do Instituto Oswaldo Cruz, 98(5), 665-672 (2003-09-16)
The way in which vectors distribute themselves amongst their hosts has important epidemiological consequences. While the role played by active host choice is largely unquestioned, current knowledge relates mostly to the innate response of vectors towards stimuli signalling the presence
A Route to the Thapsigargins from (S)-Carvone Providing a Substrate-Controlled Total Synthesis of Trilobolide, Nortrilobolide, and Thapsivillosin F
Oliver SF, et al.
Angewandte Chemie (International Edition in English), 42(48), 5996-6000 (2003)
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