6-bromo-N-methyltryptamine

Base Information

Chemical Name:6-bromo-N-methyltryptamine
CAS No.:209169-05-1
Molecular Formula:C11H13BrN2
Molecular Weight:253.13832
Hs Code.:2933990090
DSSTox Substance ID:DTXSID10448550
Nikkaji Number:J2.971.897K
Wikidata:Q27137400
Metabolomics Workbench ID:125159
ChEMBL ID:CHEMBL1835614
Mol file:209169-05-1.mol

Synonyms:6-bromo-N-methyltryptamine;209169-05-1;2-(6-bromo-1H-indol-3-yl)-N-methylethanamine;CHEMBL1835614;CHEBI:69059;2-(6-bromo-1H-indol-3-yl)-N-methylethan-1-amine;1H-Indole-3-ethanamine, 6-bromo-N-methyl-;AMY2003;DTXSID10448550;BDBM50419274;2-(6-bromo-1H-indol-3-yl)-N-methyl ethanamine;Q27137400;[2-(6-BROMO-1H-INDOL-3-YL)ETHYL](METHYL)AMINE

Suppliers and Price of 6-bromo-N-methyltryptamine

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

Chemenu
2-(6-bromo-1H-indol-3-yl)-N-methylethan-1-amine 95%
1g
$ 505.00

Alichem
2-(6-Bromo-1H-indol-3-yl)-N-methylethanamine
1g
$ 440.36

Total 3 raw suppliers

Chemical Property of 6-bromo-N-methyltryptamine

Chemical Property:

PSA：27.82000
LogP:3.08320
XLogP3:3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:252.02621
Heavy Atom Count:14
Complexity:186

Purity/Quality:

95+% ^*data from raw suppliers

2-(6-bromo-1H-indol-3-yl)-N-methylethan-1-amine 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNCCC1=CNC2=C1C=CC(=C2)Br

Technology Process of 6-bromo-N-methyltryptamine

There total 6 articles about 6-bromo-N-methyltryptamine 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: 82.0%

: 1352956-47-8
methyl 6-bromo-2-(1,1-dimethylallyl)-3-indoleacetate

: 209169-05-1
N-Methyl-6-bromotryptamine

Guidance literature:: With alane-N,N-dimethylethylamine complex; In tetrahydrofuran; toluene; for 3h; Reflux;
DOI:10.1246/cl.2011.1079

Reference yield: 64.0%

: 2-(6-bromoindol-3-yl)-N-methyl-2-oxoacetamide

: 209169-05-1
N-Methyl-6-bromotryptamine

Guidance literature:: With DMEA-alane; In tetrahydrofuran; toluene; Heating;
DOI:10.1016/j.bmcl.2007.06.047

Reference yield:

: 947605-02-9
methyl (2,6-dibromo-1H-indol-3-yl)acetate

: 209169-05-1
N-Methyl-6-bromotryptamine

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride; zinc/copper couple / methanol; water / 4.5 h / Reflux

2: methanol / 23 h / 65 °C

3: alane-N,N-dimethylethylamine complex / tetrahydrofuran; toluene / 3 h / Reflux

With hydrogenchloride; alane-N,N-dimethylethylamine complex; zinc/copper couple; In tetrahydrofuran; methanol; water; toluene;
DOI:10.1246/cl.2011.1079