4-Bromo-3,5-dimethoxyamphetamine

Base Information

Chemical Name:4-Bromo-3,5-dimethoxyamphetamine
CAS No.:32156-34-6
Molecular Formula:C₁₁H₁₆BrNO₂
Molecular Weight:274.158
Hs Code.:
UNII:5BN3H3UZ8R
DSSTox Substance ID:DTXSID30276857
Wikipedia:4-Bromo-3,5-dimethoxyamphetamine
Wikidata:Q4637107
ChEMBL ID:CHEMBL104362

Synonyms:4-Bromo-3,5-dimethoxyamphetamine;1-(4-bromo-3,5-dimethoxyphenyl)propan-2-amine;3,5-dimethoxy-4-bromoamphetamine;5BN3H3UZ8R;32156-34-6;UNII-5BN3H3UZ8R;Benzeneethanamine, 4-bromo-3,5-dimethoxy-alpha-methyl-;CHEMBL104362;4-Bromo-3,5-dimethoxy-alpha-methylbenzeneethanamine;Phenethylamine, 4-bromo-3,5-dimethoxy-alpha-methyl-;SCHEMBL5300674;DTXSID30276857;4-BR-3,5-DMA;BDBM50091066;Q4637107;2-(4-Bromo-3,5-dimethoxy-phenyl)-1-methyl-ethylamine;4-BROMO-3,5-DIMETHOXY-.ALPHA.-METHYLBENZENEETHANAMINE;PHENETHYLAMINE, 4-BROMO-3,5-DIMETHOXY-.ALPHA.-METHYL-;BENZENEETHANAMINE, 4-BROMO-3,5-DIMETHOXY-.ALPHA.-METHYL-

Suppliers and Price of 4-Bromo-3,5-dimethoxyamphetamine

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

Total 0 raw suppliers

Chemical Property of 4-Bromo-3,5-dimethoxyamphetamine

Chemical Property:

Boiling Point:351.5±37.0 °C(Predicted)
Density:1.324±0.06 g/cm3(Predicted)
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:273.03644
Heavy Atom Count:15
Complexity:177

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CC1=CC(=C(C(=C1)OC)Br)OC)N

Technology Process of 4-Bromo-3,5-dimethoxyamphetamine

There total 4 articles about 4-Bromo-3,5-dimethoxyamphetamine 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:

: 56518-42-4
4-bromo-3,5-dimethoxybenzoic acid

: 32156-34-6
4-bromo-3,5-dimethoxyphenylisopropylamine

Guidance literature:: Multi-step reaction with 3 steps

1: (i) SOCl₂, (ii) Li

2: NH₄OAc / acetic acid

3: LiAlH₄

With lithium aluminium tetrahydride; ammonium acetate; In acetic acid;
DOI:10.1021/jm00286a026

Reference yield:

: 31558-40-4
4-bromo-3,5-dimethoxybenzaldehyde

: 32156-34-6
4-bromo-3,5-dimethoxyphenylisopropylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 57 percent / NH₄OAc / 5 h / Heating

2: LiAlH₄; AlCl₃ / tetrahydrofuran; diethyl ether / 1 h / Heating

With lithium aluminium tetrahydride; aluminium trichloride; ammonium acetate; In tetrahydrofuran; diethyl ether; 1: Condensation / 2: Reduction;
DOI:10.1021/jm9906062

Reference yield:

: 31558-32-4
(+/-)-1-(4-bromo-3,5-dimethoxyphenyl)-2-nitropropene

: 32156-34-6
4-bromo-3,5-dimethoxyphenylisopropylamine

Guidance literature:: With lithium aluminium tetrahydride; aluminium trichloride; In tetrahydrofuran; diethyl ether; for 1h; Heating;
DOI:10.1021/jm9906062