2-(9H-beta-Carbolin-1-yl)ethanol

Base Information

Chemical Name:2-(9H-beta-Carbolin-1-yl)ethanol
CAS No.:102828-03-5
Molecular Formula:C₁₃H₁₂N₂O
Molecular Weight:212.251
Hs Code.:
DSSTox Substance ID:DTXSID20145528
Nikkaji Number:J389.849K
Wikidata:Q83010098
Mol file:102828-03-5.mol

Synonyms:2-(9H-beta-Carbolin-1-yl)ethanol;2-(9H-pyrido[3,4-b]indol-1-yl)ethanol;102828-03-5;1-(2'-Hydroxyethyl)-beta-carboline;beta-Carboline-1-ethanol;DTXSID20145528

Suppliers and Price of 2-(9H-beta-Carbolin-1-yl)ethanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-(9H-beta-Carbolin-1-yl)ethanol

Chemical Property:

Vapor Pressure:2.8E-09mmHg at 25°C
XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:212.094963011
Heavy Atom Count:16
Complexity:246

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)CCO

Technology Process of 2-(9H-beta-Carbolin-1-yl)ethanol

There total 5 articles about 2-(9H-beta-Carbolin-1-yl)ethanol 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: 98.0%

: 126412-15-5
1-(ethoxycarbonylmethyl)-β-carboline

: 102828-03-5
1-(2-Hydroxyethyl)-β-carboline

Guidance literature:: DOI:10.1016/S0040-4039(01)89018-3

Reference yield:

: 61-54-1
tryptamine

: 102828-03-5
1-(2-Hydroxyethyl)-β-carboline

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / aq. NaOH / CH₂Cl₂ / 1 h / Ambient temperature

2: 61 percent / POCl₃ / 12 h / Ambient temperature

3: 10percent Pd-C / various solvent(s) / 0.17 h / 160 - 170 °C

4: 93 percent / LiAlH₄ / tetrahydrofuran / 2 h / Ambient temperature

With sodium hydroxide; lithium aluminium tetrahydride; trichlorophosphate; palladium on activated charcoal; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(01)91003-8

Reference yield:

: 126412-13-3
ethyl 3-{[2-(1H-indol-3-yl)ethyl]amino}-3-oxopropanoate

: 102828-03-5
1-(2-Hydroxyethyl)-β-carboline

Guidance literature:: Multi-step reaction with 3 steps

1: 61 percent / POCl₃ / 12 h / Ambient temperature

2: 10percent Pd-C / various solvent(s) / 0.17 h / 160 - 170 °C

3: 93 percent / LiAlH₄ / tetrahydrofuran / 2 h / Ambient temperature

With lithium aluminium tetrahydride; trichlorophosphate; palladium on activated charcoal; In tetrahydrofuran;
DOI:10.1016/S0040-4020(01)91003-8