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3-Hydroxymethyl-beta-carboline

Base Information Edit
  • Chemical Name:3-Hydroxymethyl-beta-carboline
  • CAS No.:65474-79-5
  • Molecular Formula:C12H10N2O
  • Molecular Weight:198.224
  • Hs Code.:2933990090
  • European Community (EC) Number:817-069-5
  • UNII:00QJ5EQT3E
  • DSSTox Substance ID:DTXSID20215795
  • Nikkaji Number:J546.806J
  • Wikidata:Q27195268
  • ChEMBL ID:CHEMBL417982,CHEMBL1608978
  • Mol file:65474-79-5.mol
3-Hydroxymethyl-beta-carboline

Synonyms:3-hydroxymethyl-beta-carboline

Suppliers and Price of 3-Hydroxymethyl-beta-carboline
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
  • 9H-pyrido[3,4-b]indol-3-ylmethanol
  • 25mg
  • $ 220.00
  • AK Scientific
  • 3-Hydroxymethyl-beta-carboline
  • 250mg
  • $ 749.00
Total 7 raw suppliers
Chemical Property of 3-Hydroxymethyl-beta-carboline Edit
Chemical Property:
  • Appearance/Colour:Yellow solid 
  • Vapor Pressure:1.74E-09mmHg at 25°C 
  • Melting Point:225-228° 
  • Refractive Index:1.795 
  • Boiling Point:466 °C at 760 mmHg 
  • PKA:13?+-.0.10(Predicted) 
  • Flash Point:235.6 °C 
  • PSA:48.91000 
  • Density:1.385 g/cm3 
  • LogP:2.20840 
  • XLogP3:2.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:198.079312947
  • Heavy Atom Count:15
  • Complexity:234
Purity/Quality:

99% *data from raw suppliers

9H-pyrido[3,4-b]indol-3-ylmethanol *data from reagent suppliers

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

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C3=C(N2)C=NC(=C3)CO
  • Uses As tools for studying benzodiazepine receptors.
Technology Process of 3-Hydroxymethyl-beta-carboline

There total 12 articles about 3-Hydroxymethyl-beta-carboline 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 lithium aluminium tetrahydride; water; In tetrahydrofuran; at 0 - 20 ℃; for 2h; Reagent/catalyst; Solvent;
Guidance literature:
ethyl 9H-pyrido[3,4-b]indole-3-carboxylate; With lithium borohydride; In tetrahydrofuran; at 20 ℃; for 9h;
With water; In tetrahydrofuran; at 20 ℃;
Guidance literature:
Multi-step reaction with 4 steps
1: sodium hydroxide / water / 37 °C
2: thionyl chloride / 2 h / Reflux
3: manganese(IV) oxide / toluene / 16 h / 90 - 100 °C
4: lithium aluminium tetrahydride / tetrahydrofuran / 16 h / Reflux
With manganese(IV) oxide; lithium aluminium tetrahydride; thionyl chloride; sodium hydroxide; In tetrahydrofuran; water; toluene;
DOI:10.1016/j.bmcl.2015.07.058
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