2,4,5-Trihydroxyamphetamine

Base Information

Chemical Name:2,4,5-Trihydroxyamphetamine
CAS No.:41241-36-5
Molecular Formula:C9H13NO3
Molecular Weight:183.207
Hs Code.:
UNII:C6JI2489W2
DSSTox Substance ID:DTXSID90897244
Nikkaji Number:J718.530H
Wikipedia:2,4,5-Trihydroxyamphetamine
Wikidata:Q21099618
ChEMBL ID:CHEMBL28225
Mol file:41241-36-5.mol

Synonyms:2,4,5-trihydroxyamphetamine;tri-HO-A

Suppliers and Price of 2,4,5-Trihydroxyamphetamine

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 2,4,5-Trihydroxyamphetamine

Chemical Property:

Boiling Point:399.5°Cat760mmHg
Flash Point:195.4°C
Density:1.326g/cm³
XLogP3:0.6
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:183.08954328
Heavy Atom Count:13
Complexity:165

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CC1=CC(=C(C=C1O)O)O)N

Technology Process of 2,4,5-Trihydroxyamphetamine

There total 4 articles about 2,4,5-Trihydroxyamphetamine 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: 7.2%

: 555-64-6,14513-20-3
α-methyldopamine

: 3131-52-0
1H-indole-5,6-diol

: 41241-36-5,136706-33-7
1-(2,4,5-trihydroxyphenyl)-2-aminopropane

: 6-nitrodopamine

Guidance literature:: With dihydrogen peroxide; horseradish peroxidase; sodium nitrite; In phosphate buffer; at 37 ℃; pH=7.4; Further Variations:; pH-values; Reagents; Product distribution; Kinetics;
DOI:10.1021/tx990121g

Reference yield:

: 4460-86-0,14374-62-0
asaraldehyde

: 41241-36-5,136706-33-7
1-(2,4,5-trihydroxyphenyl)-2-aminopropane

Guidance literature:: Multi-step reaction with 2 steps

1: NH₄OAc / acetic acid

2: (i) LiAlH₄, Et₂O, (ii) BBr₃, CH₂Cl₂

With ammonium acetate; In acetic acid;
DOI:10.1021/jm00232a007