W379401

(3aR)-(+)-Sclareolide

natural, 97%, FG

• Sinônimo(s): Sclareolide
• Fórmula empírica (Notação de Hill): C₁₆H₂₆O₂
• Número CAS: 564-20-5
• Peso molecular: 250.38
• Número FEMA: 3794
• Número CE: 209-269-0
• Número MDL: MFCD00134168
• Código UNSPSC: 12164502
• ID de substância PubChem: 329830654
• Número de Flavis: 16.055
• NACRES: NA.21
• Organoléptico: woody; paper
• grau: FG; Fragrance grade; natural
• fonte biológica: Salvia sclarea L
• Agency: follows IFRA guidelines
• alérgeno alimentar: no known allergens

Propriedades

• fonte biológica: Salvia sclarea L
• Nível de qualidade: 400
• grau: FG; Fragrance grade; natural
• Agency: follows IFRA guidelines
• conformidade reg.: EU Regulation 1223/2009; EU Regulation 1334/2008 & 872/2012; FDA 21 CFR 110
• Ensaio: 97%
• características do produto alternativo mais ecológico: Less Hazardous Chemical Syntheses; Use of Renewable Feedstocks; Learn more about the Principles of Green Chemistry.
• sustainability: Greener Alternative Product
• Impurezas: may contain ≤0.10% 2-Methylpentane (residual solvent)
• pf: 124-126 °C (lit.)
• aplicação(ões): flavors and fragrances
• Documentação: see Safety & Documentation for available documents
• alérgeno alimentar: no known allergens
• alérgeno de fragrância: sclareol
• categoria alternativa mais ecológica: Aligned
• Organoléptico: woody; paper
• cadeia de caracteres SMILES: [H][C@@]12CC[C@@]3(C)OC(=O)C[C@]3([H])[C@@]1(C)CCCC2(C)C
• InChI: 1S/C16H26O2/c1-14(2)7-5-8-15(3)11(14)6-9-16(4)12(15)10-13(17)18-16/h11-12H,5-10H2,1-4H3/t11-,12+,15-,16+/m0/s1
• chave InChI: IMKJGXCIJJXALX-SHUKQUCYSA-N

Descrição

Descrição geral

We are committed to bringing you greener alternative products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is Biobased and thus aligns with "Less Hazardous Chemical Syntheses" and "Use of Renewable Feedstocks".

Aplicação

• Approach to Merosesquiterpenes via Lewis Acid Catalyzed Nazarov-Type Cyclization.: The synthesis of "(3aR)-(+)-Sclareolide" plays a crucial role in the total synthesis of Akaol A, a merosesquiterpene. This compound is utilized in studies focusing on Lewis acid-catalyzed Nazarov-type cyclization, which is a key reaction for constructing complex cyclic structures within organic molecules. This synthesis process not only expands the capabilities of chemists to build intricate molecular architectures but also enhances the understanding of reaction mechanisms crucial for pharmaceutical development (DOI: 10.1021/acs.orglett.6b00446).

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)