W379401

(3aR)-(+)-Sclareolide

natural, 97%, FG

• Sinónimos: Sclareolide
• Fórmula empírica (notación de Hill): C₁₆H₂₆O₂
• Número de CAS: 564-20-5
• Peso molecular: 250.38
• Número de FEMA: 3794
• Número CE: 209-269-0
• Número MDL: MFCD00134168
• Código UNSPSC: 12164502
• ID de la sustancia en PubChem: 329830654
• Número Flavis: 16.055
• NACRES: NA.21

Propiedades

• origen biológico: Salvia sclarea L
• Nivel de calidad: 400
• grado: FG; Fragrance grade; natural
• Agency: follows IFRA guidelines
• cumplimiento norm.: EU Regulation 1223/2009; EU Regulation 1334/2008 & 872/2012; FDA 21 CFR 110
• Análisis: 97%
• características de los productos alternativos más sostenibles: 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)
• mp: 124-126 °C (lit.)
• aplicaciones: flavors and fragrances
• Documentación: see Safety & Documentation for available documents
• alérgeno alimentario: no known allergens
• alérgeno de la fragancia: sclareol
• categoría alternativa más sostenible: Aligned
• Organoléptico: woody; paper
• cadena 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
• Clave InChI: IMKJGXCIJJXALX-SHUKQUCYSA-N

Descripción

Descripción general

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".

Aplicación

• 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).

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 2
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Gloves, type N95 (US)