357995

Sclareol

98%

• Sinônimo(s): Labd-14-ene-8,13-diol, (1R,2R,8aS)-Decahydro-1-(3-hydroxy-3-methyl-4-pentenyl)-2,5,5,8a-tetramethyl-2-naphthol
• Fórmula empírica (Notação de Hill): C₂₀H₃₆O₂
• Número CAS: 515-03-7
• Peso molecular: 308.50
• Beilstein: 2054148
• Número CE: 208-194-0
• Número MDL: MFCD00869558
• Código UNSPSC: 12352002
• ID de substância PubChem: 24861955
• NACRES: NA.22

Propriedades

• Ensaio: 98%
• atividade óptica: [α]25/D −13°, c = 4 in carbon tetrachloride
• p.e.: 218-220 °C/19 mmHg (lit.)
• pf: 95-100 °C (lit.)
• grupo funcional: hydroxyl
• cadeia de caracteres SMILES: CC1(C)CCC[C@@]2(C)[C@H]1CC[C@@](C)(O)[C@@H]2CC[C@@](C)(O)C=C
• InChI: 1S/C20H36O2/c1-7-18(4,21)13-9-16-19(5)12-8-11-17(2,3)15(19)10-14-20(16,6)22/h7,15-16,21-22H,1,8-14H2,2-6H3/t15-,16+,18-,19-,20+/m0/s1
• chave InChI: XVULBTBTFGYVRC-HHUCQEJWSA-N

Descrição

Descrição geral

Sclareol, a diterpene compound with a labdane skeleton, is mainly used as a raw material in the fragrance industry.[1] It shows potent cytotoxic and cytostatic effect in human leukemic cell lines.[2]

Aplicação

Sclareol may be used as a starting material in the synthesis of ambergris fragrance chemicals such as ambraoxide, ambrox, methylambraoxide, ambracetal, ambraketal and epiambraketal.[3][4] It may also be used in the synthesis of (+)-galanolactone, (-)-8-epi-galanolactone and (+)-labdienedial.[5]

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 2
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable
• Equipamento de proteção individual: Eyeshields, Gloves, type N95 (US)