2-Furan-2-yl-2-(1H-indol-3-yl)-ethylamine

Base Information

Chemical Name:2-Furan-2-yl-2-(1H-indol-3-yl)-ethylamine
CAS No.:51626-51-8
Molecular Formula:C₁₄H₁₄N₂O
Molecular Weight:226.278
Hs Code.:
DSSTox Substance ID:DTXSID701295950
ChEMBL ID:CHEMBL1619933
Mol file:51626-51-8.mol

Synonyms:2-Furan-2-yl-2-(1H-indol-3-yl)-ethylamine;51626-51-8;2-(furan-2-yl)-2-(1H-indol-3-yl)ethanamine;1H-Indole-3-ethanamine, beta-2-furanyl-;Oprea1_011674;Oprea1_855469;IFLab1_003451;CHEMBL1619933;DTXSID701295950;HMS1421M19;AKOS000301227;AKOS022211595;CCG-147317;beta-2-Furanyl-1H-indole-3-ethanamine;2-(2-furyl)-2-(indol-3-yl)ethylamine;SR-01000393618;SR-01000393618-1;2-furan-2-yl-2-(1H-indol-3-yl)-ethylamine, AldrichCPR

Suppliers and Price of 2-Furan-2-yl-2-(1H-indol-3-yl)-ethylamine

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

Matrix Scientific
2-Furan-2-yl-2-(1H-indol-3-yl)-ethylamine
1g
$ 400.00

American Custom Chemicals Corporation
2-FURAN-2-YL-2-(1H-INDOL-3-YL)-ETHYLAMINE 95.00%
500MG
$ 777.32

Total 6 raw suppliers

Chemical Property of 2-Furan-2-yl-2-(1H-indol-3-yl)-ethylamine

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:226.110613074
Heavy Atom Count:17
Complexity:259

Purity/Quality:

98%min ^*data from raw suppliers

2-Furan-2-yl-2-(1H-indol-3-yl)-ethylamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi,T
Statements: 25
Safety Statements: 45

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=CN2)C(CN)C3=CC=CO3

Technology Process of 2-Furan-2-yl-2-(1H-indol-3-yl)-ethylamine

There total 5 articles about 2-Furan-2-yl-2-(1H-indol-3-yl)-ethylamine 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: 95.0%

: 51626-49-4
3-(1-furan-2-yl-2-nitro-ethyl)-indole

: 51626-51-8
2-(furan-2-yl)-2-(1H-indol-3-yl)ethanamine

Guidance literature:: With sodium tetrahydroborate; nickel(II) chloride hexahydrate; In methanol; at 0 ℃; for 0.5h; Inert atmosphere; Schlenk technique;
DOI:10.1039/d0cc00321b

Reference yield:

: 120-72-9
indole

: 51626-51-8
2-(furan-2-yl)-2-(1H-indol-3-yl)ethanamine

Guidance literature:: Multi-step reaction with 2 steps

1: HCO₂H / 4 h / Ambient temperature

2: LiAlH₄ / diethyl ether / Heating

With lithium aluminium tetrahydride; formic acid; In diethyl ether;
DOI:10.1007/BF00470346

Reference yield:

: 699-18-3,32782-45-9
2-(2-nitrovinyl)furan

: 51626-51-8
2-(furan-2-yl)-2-(1H-indol-3-yl)ethanamine

Guidance literature:: Multi-step reaction with 2 steps

1: HCO₂H / 4 h / Ambient temperature

2: LiAlH₄ / diethyl ether / Heating

With lithium aluminium tetrahydride; formic acid; In diethyl ether;
DOI:10.1007/BF00470346