2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline

Base Information

Chemical Name:2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline
CAS No.:147293-14-9
Molecular Formula:C₁₁H₁₀N₄
Molecular Weight:198.227
Hs Code.:2933998090
European Community (EC) Number:815-053-2
DSSTox Substance ID:DTXSID40163648
Nikkaji Number:J566.150A
Wikidata:Q83032617
Mol file:147293-14-9.mol

Synonyms:147293-14-9;2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline;3-methylimidazo[4,5-h]isoquinolin-2-amine;CCRIS 6828;3H-Imidazo(4,5-h)isoquinolin-2-amine, 3-methyl-;3-Methyl-3H-imidazo(4,5-h)isoquinolin-2-amine;2-Amino-3-methyl-3H-imidazo(4,5-h)isoquinoline;3H-Imidazo[4,5-h]isoquinolin-2-amine, 3-methyl-;3-METHYL-3H-IMIDAZO[4,5-H]ISOQUINOLIN-2-AMINE;DTXSID40163648;MFCD00468058;AKOS030240027;LS-77877;FT-0661915;J-008341;333458-15-4

Suppliers and Price of 2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline

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

TRC
2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline
50mg
$ 205.00

Medical Isotopes, Inc.
2-Amino-3-methyl-3H-imidazo[4,5-H]isoquinoline
25 mg
$ 825.00

Biosynth Carbosynth
2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline
25 mg
$ 255.00

Biosynth Carbosynth
2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline
10 mg
$ 185.00

Biosynth Carbosynth
2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline
50 mg
$ 450.00

Biosynth Carbosynth
2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline
250 mg
$ 1375.00

Biosynth Carbosynth
2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline
100 mg
$ 705.00

American Custom Chemicals Corporation
2-AMINO-3-METHYL-3H-IMIDAZO[4,5-H]ISOQUINOLINE 95.00%
25MG
$ 650.27

AK Scientific
2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline
100mg
$ 1001.00

AK Scientific
2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline
10mg
$ 299.00

Total 7 raw suppliers

Chemical Property of 2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline

Chemical Property:

Vapor Pressure:2.94E-09mmHg at 25°C
Refractive Index:1.754
Boiling Point:476.9 °C at 760 mmHg
Flash Point:242.2 °C
PSA：56.73000
Density:1.41 g/cm³
LogP:2.28490
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:198.090546336
Heavy Atom Count:15
Complexity:245

Purity/Quality:

99% ^*data from raw suppliers

2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2=C(C3=C(C=C2)C=CN=C3)N=C1N
Uses As a closely related isomer to the heterocyclic food mutagen IQ, 2-Amino-3-methyl-3H-imidazo[4,5-H]isoquinoline can be useful for biological and structure-activity studies of IQ

Technology Process of 2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline

There total 4 articles about 2-Amino-3-methyl-3H-imidazo[4,5-h]isoquinoline 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: 31.0%

: 506-68-3
bromocyane

: N⁷-Methyl-isoquinoline-7,8-diamine

: 147293-14-9
2-amino-3-methyl-3H-imidazo<4,5-h>isoquinoline

Guidance literature:: In acetonitrile;

Reference yield:

: 39989-39-4
7-methoxyisoquinoline

: 147293-14-9
2-amino-3-methyl-3H-imidazo<4,5-h>isoquinoline

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / KNO₃, conc. H₂SO₄ / 24 h / 20 °C

2: 85 percent / H₂O

3: H₂ / Ni

4: 31 percent / acetonitrile

With sulfuric acid; hydrogen; potassium nitrate; nickel; In water; acetonitrile;

Reference yield:

: 63485-75-6
7-methoxy-8-nitro-isoquinoline

: 147293-14-9
2-amino-3-methyl-3H-imidazo<4,5-h>isoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / H₂O

2: H₂ / Ni

3: 31 percent / acetonitrile

With hydrogen; nickel; In water; acetonitrile;