1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-2-phenyl-

Base Information

Chemical Name:1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-2-phenyl-
CAS No.:17375-63-2
Molecular Formula:C19H22N2O
Molecular Weight:294.396
Hs Code.:
UNII:6G5F6ESV5I
Nikkaji Number:J1.303.798A
Wikidata:Q27087726
Pharos Ligand ID:8U8M3WT848ZZ
ChEMBL ID:CHEMBL7318
Mol file:17375-63-2.mol

Synonyms:5-methoxy-2-phenyl-N,N-dimethyltryptamine;BGC20-761;PMDT cpd

Suppliers and Price of 1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-2-phenyl-

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

Usbiological
BGC 20-761
10mg
$ 446.00

TRC
BGC20-761
1mg
$ 105.00

Tocris
BGC20-761 ≥98%(HPLC)
10
$ 185.00

ApexBio Technology
BGC20-761
10mg
$ 282.00

American Custom Chemicals Corporation
BGC 20-761 95.00%
5MG
$ 505.35

Total 5 raw suppliers

Chemical Property of 1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-2-phenyl-

Chemical Property:

PSA：28.26000
LogP:3.94760
Storage Temp.:Store at +4°C
Solubility.:<14.72mg/ml in ethanol; <29.44mg/ml in DMSO
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:294.173213330
Heavy Atom Count:22
Complexity:340

Purity/Quality:

≥98% by HPLC ^*data from raw suppliers

BGC 20-761 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)CCC1=C(NC2=C1C=C(C=C2)OC)C3=CC=CC=C3
Uses BGC 20-761, is a selective high affinity 5-HT6 antagonist (Ki = 20 nM). that has shown to enhance memory consolidation in a rat model. It reverses he amnesic effects of Scopolamine (S200000).

Technology Process of 1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-2-phenyl-

There total 2 articles about 1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-2-phenyl- 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: 63.0%