1H-Perimidin-2-amine

Base Information

Chemical Name:1H-Perimidin-2-amine
CAS No.:28832-64-6
Molecular Formula:C11H9 N3
Molecular Weight:183.213
Hs Code.:2933990090
European Community (EC) Number:249-264-0
DSSTox Substance ID:DTXSID1067419
Nikkaji Number:J20.224J
Wikidata:Q27452326
ChEMBL ID:CHEMBL311074
Mol file:28832-64-6.mol

Synonyms:2-aminoperimidine

Suppliers and Price of 1H-Perimidin-2-amine

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 8 raw suppliers

Chemical Property of 1H-Perimidin-2-amine

Chemical Property:

Melting Point:239°C
Refractive Index:1.6500 (estimate)
Boiling Point:421.7°Cat760mmHg
PKA:7.92±0.20(Predicted)
Flash Point:208.8°C
PSA：54.70000
Density:1.4g/cm³
LogP:2.87950
XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:183.079647300
Heavy Atom Count:14
Complexity:261

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C3C(=C1)NC(=NC3=CC=C2)N

Technology Process of 1H-Perimidin-2-amine

There total 6 articles about 1H-Perimidin-2-amine 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:

: 479-27-6
naphthalene-1,8-diamine

: 28832-64-6
1H-perimidin-2-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 1,2-dimethoxy-ethane / 1 h / Ambient temperature

2: aqueous ammonia

With ammonium hydroxide; In 1,2-dimethoxyethane;
DOI:10.1002/mrc.1260260304