Fungisterol

Base Information

• Chemical Name: Fungisterol
• CAS No.: 516-78-9
• Molecular Formula: C28H48 O
• Molecular Weight: 400.689
• European Community (EC) Number: 208-225-8
• UNII: XM6JVX97IY
• DSSTox Substance ID: DTXSID201026572
• Nikkaji Number: J16.118G
• Wikipedia: Fungisterol
• Wikidata: Q15410967
• Metabolomics Workbench ID: 34768
• Mol file: 516-78-9.mol

Synonyms:Fungisterol;gamma-Ergostenol;516-78-9;5-alpha-Ergost-7-en-3-beta-ol;7-Ergostenol;delta7-Campesterol;delta7-Campestenol;UNII-XM6JVX97IY;XM6JVX97IY;5apha-ergost-7-en-3beta-ol;EINECS 208-225-8;(3S,5S,9R,10S,13R,14R,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol;.gamma.-Ergostenol;.delta.7-Campestenol;5.alpha.-Ergost-7-en-3.beta.-ol;Delta(7)-ergostenol;Ergost-7-en-3-ol, (3.beta.,5.alpha.)-;FUNGISTEROL [MI];5alpha-Ergost-7-en-3beta-ol;SCHEMBL4434556;CHEBI:69432;(5alpha)-ergost-7beta-en-3-ol;.GAMMA.-ERGOSTENOL [MI];C28H48O;DTXSID201026572;LMST01030105;(3-beta,5-alpha)-Ergosta-7-en-3-ol;(24S)-ERGOST-7-EN-3.BETA.-OL;Q15410967;(24S)-24-METHYL-5.ALPHA.-CHOLEST-7-EN-3.BETA.-OL;(3S,5S,9R,10S,13R,14R,17R)-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-10,13-dimethyl-17-((2R,5S)-5,6-dimethylheptan-2-yl)-1H-cyclopenta[a]phenanthren-3-ol

Chemical Property of Fungisterol

Chemical Property:

• Vapor Pressure: 1.39E-11mmHg at 25°C
• Melting Point: 146°
• Refractive Index: 1.5100 (estimate)
• Boiling Point: 488.3°Cat760mmHg
• PKA: 15.10±0.70(Predicted)
• Flash Point: 214°C
• PSA: 20.23000
• Density: 0.98g/cm³
• LogP: 7.63470
• XLogP3: 8.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 400.370516150
• Heavy Atom Count: 29
• Complexity: 620

Purity/Quality:

98%min ^*data from raw suppliers

Fungisterol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C
• Isomeric SMILES: C[C@H](CC[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C
• Uses: Fungisterol is used in the improvement of the measuring methods of composition and total contents of sterols in vegetable oils, study on the antioxidant and antimicrobial activities of supercritical fluid extract of Agaricus brasiliensis.

Technology Process of Fungisterol

There total 18 articles about Fungisterol 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:

(22E)-ergosta-7,22-dien-3β-ol (2465-11-4) → (3β,5α)-ergost-7-en-3-ol (516-78-9)

Guidance literature:

With hydrogen; Wilkinson's catalyst; In benzene; for 16h;

Reference yield:

(24S)-ergosta-5,7-diene-3β-ol (20304-51-2,38521-88-9,516-79-0) → (3β,5α)-ergost-7-en-3-ol (516-78-9)

Guidance literature:

With propan-1-ol; sodium;

Reference yield:

→ (3β,5α)-ergost-7-en-3-ol (516-78-9)

Guidance literature:

With ethyl acetate; platinum; Hydrogenation_.Erwaermen des Reaktionsprodukts mit methanol. KOH;

upstream raw materials:

(24S)-ergosta-5,7-diene-3β-ol

5-dihydroergosteryl acetate

(22E)-ergosta-7,22-dien-3β-ol

propan-1-ol

Downstream raw materials:

(3β,5α)-ergost-8(14)-en-3-ol

3β-(toluene-sulfonyl-(4)-oxy)-5α-ergostene-(8(14))

5α-Ergost-8(14)-en

3β-benzyloxy-5α,8α-ergostane-7α,8-diol

Refernces

• 1、 Protiva, Jiri,Skorkovska, Hana,Urban, Jiri,Vystrcil, Alois. "TRITERPENES AND STEROIDS FROM Ganoderma applanatum". . p. 2710 - 2713. Retrieved 2007/10/02.