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Pharmakon1600-01500380

Base Information
  • Chemical Name:Pharmakon1600-01500380
  • CAS No.:2668-66-8
  • Molecular Formula:C22H32 O3
  • Molecular Weight:344.494
  • Hs Code.:
  • NSC Number:757096
  • Mol file:2668-66-8.mol
Pharmakon1600-01500380

Synonyms:Spectrum_000897;Spectrum2_000141;Spectrum3_000488;Spectrum4_000040;Spectrum5_000946;BSPBio_001955;KBioGR_000479;KBioSS_001377;DivK1c_000349;SPECTRUM1500380;SPBio_000242;SCHEMBL12998543;HMS501B11;KBio1_000349;KBio2_001377;KBio2_003945;KBio2_006513;KBio3_001455;NINDS_000349;HMS1920J21;HMS2091B12;Pharmakon1600-01500380;CCG-38940;NSC757096;NSC-757096;IDI1_000349;NCGC00178898-01;SBI-0051435.P003;AB00052035_02;SR-05000001665;SR-05000001665-1;BRD-A20126139-001-02-6;BRD-A20126139-001-03-4

Suppliers and Price of Pharmakon1600-01500380
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Medrysone
  • 25mg
  • $ 80.00
  • Sigma-Aldrich
  • 6α-Methyl-11β-hydroxyprogesterone
  • 250mg
  • $ 71.70
  • Crysdot
  • Medrysone 98+%
  • 100mg
  • $ 50.00
  • Cayman Chemical
  • 6α-methyl-11β-Hydroxyprogesterone ≥95%
  • 500mg
  • $ 85.00
  • Cayman Chemical
  • 6α-methyl-11β-Hydroxyprogesterone ≥95%
  • 250mg
  • $ 46.00
  • Cayman Chemical
  • 6α-methyl-11β-Hydroxyprogesterone ≥95%
  • 100mg
  • $ 26.00
  • ApexBio Technology
  • 6α-methyl-11β-Hydroxyprogesterone
  • 250mg
  • $ 64.00
  • ApexBio Technology
  • 6α-methyl-11β-Hydroxyprogesterone
  • 500mg
  • $ 118.00
  • American Custom Chemicals Corporation
  • MEDRYSONE 95.00%
  • 100MG
  • $ 885.31
  • AK Scientific
  • Medrysone
  • 100mg
  • $ 135.00
Total 14 raw suppliers
Chemical Property of Pharmakon1600-01500380
Chemical Property:
  • Vapor Pressure:9.3E-12mmHg at 25°C 
  • Melting Point:155-158° 
  • Boiling Point:492.3°Cat760mmHg 
  • PKA:14.53±0.70(Predicted) 
  • Flash Point:265.7°C 
  • PSA:54.37000 
  • Density:1.13g/cm3 
  • LogP:3.94030 
  • Storage Temp.:2-8°C 
  • Solubility.:Acetone (Slightly), Chloroform (Slightly), Methanol (Slightly, Sonicated) 
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:344.23514488
  • Heavy Atom Count:25
  • Complexity:650
Purity/Quality:

97% *data from raw suppliers

Medrysone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1CC2C3CCC(C3(CC(C2C4(C1=CC(=O)CC4)C)O)C)C(=O)C
  • Isomeric SMILES:C[C@H]1CC2C3CC[C@@H]([C@]3(C[C@@H](C2[C@@]4(C1=CC(=O)CC4)C)O)C)C(=O)C
  • Description 6α-methyl-11β-hydroxy Progesterone is an anti-inflammatory steroid. It is a hydroxylated progesterone that lacks progestational and androgenic activity. It inhibits phytohemagglutinin-activated T cell proliferation in vitro with an IC50 value of 2.9 μg/ml. 6α-methyl-11β-hydroxy Progesterone also inhibits TNF-α production in LPS-stimulated THP-1 cells (IC50 = 30.54 μg/ml). Topical formulations containing 6α-methyl-11β-hydroxyprogesterone have been used to treat inflammatory ocular diseases.
  • Uses glucocorticoid Medrysone is a corticosteroid that is seen to increase intraocular pressure.
  • Therapeutic Function Glucocorticoid
Technology Process of Pharmakon1600-01500380

There total 5 articles about Pharmakon1600-01500380 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:
Guidance literature:
With tetrahydrofuran; lithium aluminium tetrahydride; diethyl ether; Erwaermen des Reaktionsprodukts mit wss.-methanol.H2SO4;
Guidance literature:
Multi-step reaction with 2 steps
1: benzene; toluene-4-sulfonic acid / unter Entfernen des entstehenden Wassers
2: LiAlH4; THF; diethyl ether / Erwaermen des Reaktionsprodukts mit wss.-methanol.H2SO4
With tetrahydrofuran; lithium aluminium tetrahydride; diethyl ether; toluene-4-sulfonic acid; benzene;

Reference yield:

Guidance literature:
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