2,5-Dimethoxy-4-nitroamphetamine

Base Information

Chemical Name:2,5-Dimethoxy-4-nitroamphetamine
CAS No.:67460-68-8
Molecular Formula:C11H16N2O4
Molecular Weight:240.259
Hs Code.:
UNII:3FIV60666J
DSSTox Substance ID:DTXSID00874243
Nikkaji Number:J275.080E
Wikipedia:2,5-Dimethoxy-4-nitroamphetamine
Wikidata:Q4596794
ChEMBL ID:CHEMBL8301

Synonyms:1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropane;1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropane monohydrochloride, (+-)-isomer;1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropane monohydrochloride, (R)-isomer;1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropane, (+-)-isomer;1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropane, (R)-isomer

Suppliers and Price of 2,5-Dimethoxy-4-nitroamphetamine

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 27 raw suppliers

Chemical Property of 2,5-Dimethoxy-4-nitroamphetamine

Chemical Property:

Vapor Pressure:1.56E-06mmHg at 25°C
Boiling Point:397.6°C at 760 mmHg
Flash Point:194.3°C
PSA：90.30000
Density:1.185g/cm³
LogP:2.72520
XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:240.11100700
Heavy Atom Count:17
Complexity:256

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CC1=CC(=C(C=C1OC)[N+](=O)[O-])OC)N

Technology Process of 2,5-Dimethoxy-4-nitroamphetamine

There total 6 articles about 2,5-Dimethoxy-4-nitroamphetamine 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:

: 2801-68-5
2,5-dimethoxyphenylisopropylamine

: 67460-68-8
1-(2,5-dimethoxy-4-nitrophenyl) propan-2-amine

Guidance literature:: With nitric acid; In acetic acid; at 0 - 5 ℃;
DOI:10.1021/jm00352a013

Reference yield:

: 42203-72-5
N-Acetyl-1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropan

: 67460-68-8
1-(2,5-dimethoxy-4-nitrophenyl) propan-2-amine

Guidance literature:: With sodium hydroxide; In ethylene glycol; Heating;
DOI:10.1139/v73-210

Reference yield:

: 42311-16-0
(+/-)-N-acetyl-1-(2,5-dimethoxyphenyl)-2-aminopropane

: 67460-68-8
1-(2,5-dimethoxy-4-nitrophenyl) propan-2-amine

Guidance literature:: Multi-step reaction with 2 steps

1: aq. HNO₃, NaNO₂ / acetic acid

2: aq. NaOH / ethane-1,2-diol / Heating

With sodium hydroxide; nitric acid; sodium nitrite; In ethylene glycol; acetic acid;
DOI:10.1139/v73-210