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(1S,4S,7S,8S,11S,12R,13S)-2,12-Dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one

Base Information Edit
  • Chemical Name:(1S,4S,7S,8S,11S,12R,13S)-2,12-Dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one
  • CAS No.:2115-91-5
  • Molecular Formula:C16H25NO2
  • Molecular Weight:263.38
  • Hs Code.:29399990
  • DSSTox Substance ID:DTXSID70896917
  • Wikipedia:Dendrobine
  • Wikidata:Q76149937
  • Mol file:2115-91-5.mol
(1S,4S,7S,8S,11S,12R,13S)-2,12-Dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one

Synonyms:dendrobine;dendrobine hydrochloride

Suppliers and Price of (1S,4S,7S,8S,11S,12R,13S)-2,12-Dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one
Supply Marketing:Edit
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
  • Dendrobine
  • 10mg
  • $ 150.00
  • Medical Isotopes, Inc.
  • Dendrobine
  • 100 mg
  • $ 2200.00
  • JR MediChem
  • Dendrobine 98%
  • 20mg
  • $ 1400.00
  • DC Chemicals
  • Dendrobine >98%,StandardReferencesGrade
  • 20 mg
  • $ 280.00
  • ChemScene
  • Dendrobine ≥98.0%
  • 5mg
  • $ 178.00
  • ChemScene
  • Dendrobine ≥98.0%
  • 10mg
  • $ 303.00
  • ChemScene
  • Dendrobine ≥98.0%
  • 20mg
  • $ 514.00
  • Cayman Chemical
  • Dendrobine
  • 50mg
  • $ 595.00
  • Cayman Chemical
  • Dendrobine
  • 25mg
  • $ 340.00
  • Cayman Chemical
  • Dendrobine
  • 10mg
  • $ 153.00
Total 102 raw suppliers
Chemical Property of (1S,4S,7S,8S,11S,12R,13S)-2,12-Dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one Edit
Chemical Property:
  • Vapor Pressure:8.25E-06mmHg at 25°C 
  • Melting Point:135-136℃ 
  • Refractive Index:1.525 
  • Boiling Point:374.602 °C at 760 mmHg 
  • PKA:9.49±0.60(Predicted) 
  • Flash Point:132.762 °C 
  • PSA:29.54000 
  • Density:1.101 g/cm3 
  • LogP:2.09820 
  • XLogP3:3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:263.188529040
  • Heavy Atom Count:19
  • Complexity:435
Purity/Quality:

99% *data from raw suppliers

Dendrobine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C
  • Isomeric SMILES:CC(C)[C@H]1[C@@H]2[C@@H]3CC[C@H]4[C@@]3([C@@H]([C@H]1OC2=O)N(C4)C)C
  • Description Dendrobine is a sesquiterpenoid that has been found in D. nobile and has anticancer activity. It decreases viability of A549 cells when used at concentrations ranging from 2.5 to 15 μg/ml. It induces apoptosis in A549 cells when used at concentrations ranging from 1 to 10 μg/ml, as well as increases JNK phosphorylation and sensitizes A549 cells to cisplatin at 10 μg/ml. Dendrobine (50 mg/kg per day) reduces tumor growth in an A549 mouse xenograft model with an additive effect when used in combination with cisplatin.
  • Uses Dendrobine is an alkaloid isolated from Dendrobium nobile and is an antagonist of β-alanine, taurine and of presynaptic inhibition in the frog spinal cord.
Technology Process of (1S,4S,7S,8S,11S,12R,13S)-2,12-Dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one

There total 101 articles about (1S,4S,7S,8S,11S,12R,13S)-2,12-Dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one 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 sodium tetrahydroborate; In isopropyl alcohol; at 20 - 50 ℃; for 77h; Inert atmosphere;
DOI:10.1002/anie.201108564
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