C15 H24,

Base Information

• Chemical Name: C15 H24,
• CAS No.: 30021-74-0
• Molecular Formula: 948-32-3
• Molecular Weight: 204.356
• UNII: L2F6RNG65D
• Nikkaji Number: J259.746B
• Wikidata: Q105311286
• Mol file: 30021-74-0.mol

Synonyms:C15 H24,;(1à,4aà,8aà)-1,2,3,4,4a,5,6,8a-Octahydro-7-methyl-4-methylene-1-(1-methylethyl)-naphthalene

Chemical Property of C15 H24,

Chemical Property:

• Boiling Point: 272.1±20.0 °C(Predicted)
• PSA: 0.00000
• Density: 0.89±0.1 g/cm3(Predicted)
• LogP: 4.58110
• XLogP3: 4.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 204.187800766
• Heavy Atom Count: 15
• Complexity: 282

Purity/Quality:

99% ^*data from raw suppliers

γ-Muurolene ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1=CC2C(CC1)C(=C)CCC2C(C)C
• Isomeric SMILES: CC1=C[C@H]2[C@@H](CC1)C(=C)CC[C@@H]2C(C)C
• Uses: γ-Muurolene is a terpenoid and naturally found in the essential oil from Bulgaria and Garcinia brasiliensis. γ-Muurolene may exhibit antioxidant and anti-inflammatory activities.

Technology Process of C15 H24,

There total 23 articles about C15 H24, 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: 17.0%

germacrene D (105453-16-5) → (±)-δ-cadinene (483-76-1,13061-82-0,16729-01-4,20085-20-5,60305-17-1,73365-79-4) + epizonarene (5975-30-4,35938-51-3,36437-95-3,41702-63-0,41702-64-1,41929-05-9,51819-91-1,74036-35-4,76898-68-5,149115-45-7) + γ-cadinene (39029-41-9) + γ-muurolene (30021-74-0)

Guidance literature:

With toluene-4-sulfonic acid; In dichloromethane; at 20 ℃; Further byproducts given;

DOI:10.1016/S0031-9422(00)00266-1

Reference yield: 11.0%

germacrene D (105453-16-5) → (±)-δ-cadinene (483-76-1,13061-82-0,16729-01-4,20085-20-5,60305-17-1,73365-79-4) + γ-cadinene (39029-41-9) + γ-muurolene (30021-74-0) + opposita-4(15),7-diene

Guidance literature:

With toluene-4-sulfonic acid; In dichloromethane; at 20 ℃; Further byproducts given;

DOI:10.1016/S0031-9422(00)00266-1

Reference yield: 10.0%

germacrene D (105453-16-5) → (±)-α-cadinene (483-75-0,10208-80-7,13862-36-7,17627-24-6,20085-19-2,23515-88-0,24406-05-1,31983-21-8,31983-22-9,51260-25-4,68000-45-3,82468-90-4) + (±)-δ-cadinene (483-76-1,13061-82-0,16729-01-4,20085-20-5,60305-17-1,73365-79-4) + γ-cadinene (39029-41-9) + γ-muurolene (30021-74-0)

Guidance literature:

With boron trifluoride dimethyl etherate; In diethyl ether; Dimethyl ether; at 0 ℃; for 0.2h; Further byproducts given;

DOI:10.1016/S0031-9422(00)00266-1

upstream raw materials:

(+)-α-cadinol

vetidiol

C₁₅H₂₄O₃

C₂₉H₃₆O₇S₂