3-Phenylimidazo[1,5-a]pyrazine

Base Information

Chemical Name:3-Phenylimidazo[1,5-a]pyrazine
CAS No.:55316-37-5
Molecular Formula:C12H9 N3
Molecular Weight:195.224
Hs Code.:
NSC Number:194619
DSSTox Substance ID:DTXSID20307705
Wikidata:Q82055215

Synonyms:3-phenylimidazo[1,5-a]pyrazine;55316-37-5;NSC194619;SCHEMBL10095082;DTXSID20307705;3-phenyl-Imidazo[1,5-a]pyrazine;imidazo[1,5-a]pyrazine,3-phenyl-;NSC-194619;C91465

Suppliers and Price of 3-Phenylimidazo[1,5-a]pyrazine

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 10 raw suppliers

Chemical Property of 3-Phenylimidazo[1,5-a]pyrazine

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.21g/cm³
XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:195.079647300
Heavy Atom Count:15
Complexity:213

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NC=C3N2C=CN=C3

Technology Process of 3-Phenylimidazo[1,5-a]pyrazine

There total 4 articles about 3-Phenylimidazo[1,5-a]pyrazine 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: 92.0%

: 55316-25-1
N-pyrazin-2-ylmethyl-benzamide

: 55316-37-5
3-phenyl-imidazo[1,5-a]pyrazine

Guidance literature:: With trichlorophosphate; In acetonitrile; at 85 ℃; for 4h; Inert atmosphere;

Reference yield:

: 20010-99-5
2-aminomethylpyrazine

: 55316-37-5
3-phenyl-imidazo[1,5-a]pyrazine

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 0 - 20 °C / Inert atmosphere

2: trichlorophosphate / acetonitrile / 4 h / 85 °C / Inert atmosphere

With N-ethyl-N,N-diisopropylamine; trichlorophosphate; In dichloromethane; acetonitrile;

Reference yield:

: 98-88-4
benzoyl chloride

: 55316-37-5
3-phenyl-imidazo[1,5-a]pyrazine

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 0 - 20 °C / Inert atmosphere

2: trichlorophosphate / acetonitrile / 4 h / 85 °C / Inert atmosphere

With N-ethyl-N,N-diisopropylamine; trichlorophosphate; In dichloromethane; acetonitrile;