2,5-Dimethoxy-4-pentylamphetamine

Base Information

Chemical Name:2,5-Dimethoxy-4-pentylamphetamine
CAS No.:63779-90-8
Molecular Formula:C₁₆H₂₇NO₂
Molecular Weight:265.396
Hs Code.:2922199090
UNII:N80EWL36CB
ChEMBL ID:CHEMBL161416
DSSTox Substance ID:DTXSID50482958
Nikkaji Number:J273.477J
Wikidata:Q4596788
Wikipedia:2,5-Dimethoxy-4-amylamphetamine

Synonyms:63779-90-8;2,5-Dimethoxy-4-pentylamphetamine;2,5-Dimethoxy-4-amylamphetamine;DOAM;N80EWL36CB;1-(2,5-DIMETHOXY-4-PENTYLPHENYL)PROPAN-2-AMINE;alpha-Methyl-4-amyl-2,5-dimethoxyphenethylamine;UNII-N80EWL36CB;CHEMBL161416;SCHEMBL5305816;DTXSID50482958;NS00018002;2,5-Dimethoxy-alpha-methyl-4-pentylbenzeneethanamine;Q4596788;Benzeneethanamine, 2,5-dimethoxy-alpha-methyl-4-pentyl-;BENZENEETHANAMINE, 2,5-DIMETHOXY-.ALPHA.-METHYL-4-PENTYL-

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

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

Cayman Chemical
DOAM ≥98%
5mg
$ 163.00

Cayman Chemical
DOAM ≥98%
1mg
$ 71.00

Cayman Chemical
DOAM ≥98%
50mg
$ 1020.00

AK Scientific
2,5-Dimethoxy-4-pentylamphetamine
5mg
$ 302.00

AK Scientific
2,5-Dimethoxy-4-pentylamphetamine
1mg
$ 187.00

Total 5 raw suppliers

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

Chemical Property:

PSA：44.48000
LogP:4.02650
XLogP3:4.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:265.204179104
Heavy Atom Count:19
Complexity:235

Purity/Quality:

99% ^*data from raw suppliers

DOAM ≥98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCC1=CC(=C(C=C1OC)CC(C)N)OC
Description DOAM (Item No. 17656) is an analytical reference standard that is structurally categorized as an amphetamine. Experiments with isolated rat thoracic aorta suggested that α-Methyl-4-amyl-2,5-dimethoxyphenethylamine may act as an antagonist of the 5-HT2 receptor. This product is intended for research and forensic applications.

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

There total 5 articles about 2,5-Dimethoxy-4-pentylamphetamine 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:

: 57314-78-0
1-(2,5-Dimethoxy-4-amylphenyl)-2-nitropropen

: 63779-90-8
2,5-dimethoxy-4-amylphenylisopropylamine

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; Heating;
DOI:10.1021/jm00246a006

Reference yield:

: 57314-84-8
2,5-dimethoxy-4-pentylbenzaldehyde

: 63779-90-8
2,5-dimethoxy-4-amylphenylisopropylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 4>OAc / acetic acid / Heating

2: LiAlH₄ / diethyl ether / Heating

With lithium aluminium tetrahydride; ammonium acetate; In diethyl ether; acetic acid;
DOI:10.1021/jm00246a006

Reference yield:

: 38843-82-2
1-(2,5-dimethoxyphenyl) pentan-1-one

: 63779-90-8
2,5-dimethoxy-4-amylphenylisopropylamine

Guidance literature:: Multi-step reaction with 3 steps

1: (i) Zn-Hg, aq. HCl, EtOH, (ii) /BRN= 636496/, POCl₃

2: 4>OAc / acetic acid / Heating

3: LiAlH₄ / diethyl ether / Heating

With lithium aluminium tetrahydride; ammonium acetate; In diethyl ether; acetic acid;
DOI:10.1021/jm00246a006