Camelliagenin C

Base Information

• Chemical Name: Camelliagenin C
• CAS No.: 14440-27-8
• Molecular Formula: C₃₀H₅₀O₅
• Molecular Weight: 490.724
• Wikidata: Q105257356
• Mol file: 14440-27-8.mol

Synonyms:Camelliagenin C;14440-27-8;4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8,9-triol;(3S,4R,4Ar,6aR,6bS,8R,8aS,9S,12aS,14aR,14bR)-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8,9-triol;Theasapogenol C;CHEBI:173217

Chemical Property of Camelliagenin C

Chemical Property:

• PSA: 101.15000
• LogP: 4.05530
• XLogP3: 5.1
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• Exact Mass: 490.36582469
• Heavy Atom Count: 35
• Complexity: 899

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1)O)CO)O)C)C)(C)CO)O)C)C

Technology Process of Camelliagenin C

There total 3 articles about Camelliagenin C 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:

(4S,4aS,5R,6aS,6bR,8aR,9R,10S,12aR,12bR,14bS)-4,5,10-Trihydroxy-9-hydroxymethyl-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydro-2H-picene-4a-carbaldehyde (145940-89-2) → 3β,16α,22α,23,28-Pentahydroxy-Δ12-oleanen; Camelliagenin C; Camelliasapogenol III (14440-27-8)

Guidance literature:

With sodium tetrahydroborate; In ethanol; for 0.333333h; Ambient temperature;

DOI:10.1016/S0031-9422(00)97564-2

Reference yield:

→ 3β,16α,22α,23,28-Pentahydroxy-Δ12-oleanen; Camelliagenin C; Camelliasapogenol III (14440-27-8)

Guidance literature:

Camelliagenin B, LiAlH4;

DOI:10.1016/S0040-4039(00)90555-0

Reference yield:

→ Camellragenin C (14440-27-8)

Guidance literature:

1) Teaponin, KOH/C2H5OH, 2) Photolyse in CH3OH;

upstream raw materials:

(4S,4aS,5R,6aS,6bR,8aR,9R,10S,12aR,12bR,14bS)-4,5,10-Trihydroxy-9-hydroxymethyl-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydro-2H-picene-4a-carbaldehyde