1,2,3,4-Tetrahydropyrazino[1,2-a]benzimidazole

Base Information

Chemical Name:1,2,3,4-Tetrahydropyrazino[1,2-a]benzimidazole
CAS No.:4744-53-0
Molecular Formula:C₁₀H₁₁N₃
Molecular Weight:173.217
Hs Code.:
NSC Number:700996
DSSTox Substance ID:DTXSID601249623
Nikkaji Number:J1.675.184G
ChEMBL ID:CHEMBL6503
Mol file:4744-53-0.mol

Synonyms:1,2,3,4-tetrahydropyrazino[1,2-a]benzimidazole;4744-53-0;CHEMBL6503;1,8,11-Triazatricyclo[7.4.0.0,2,7]trideca-2,4,6,8-tetraene;NSC700996;Oprea1_448969;Oprea1_753230;SCHEMBL839815;1,2,3,4-Tetrahydro-benzo[4,5]imidazo[1,2-a]pyrazine;DTXSID601249623;HMS1607D02;BDBM50108305;Pyrazino[1,2-a]benzimidazole, 1,2,3,4-tetrahydro- (6CI,8CI,9CI);STL468855;AKOS005214675;NSC-700996;NCI60_036281;EU-0033777;EN300-225247;1,2,3,4-tetrahydrobenzo[4,5]imidazo[1,2-a]pyrazine;2,3,4,5-tetrahydro-1H-pyrazino[1,2-a]benzoimidazole;F0910-0058

Suppliers and Price of 1,2,3,4-Tetrahydropyrazino[1,2-a]benzimidazole

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

American Custom Chemicals Corporation
1,2,3,4-TETRAHYDRO-PYRAZINO[1,2-A]BENZIMIDAZOLE 95.00%
5MG
$ 497.50

AccelPharmtech
1,2,3,4-tetrahydro-Pyrazino[1,2-a]benzimidazole 97.00%
5G
$ 2330.00

Total 4 raw suppliers

Chemical Property of 1,2,3,4-Tetrahydropyrazino[1,2-a]benzimidazole

Chemical Property:

PSA：29.85000
LogP:1.46830
XLogP3:0.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:173.095297364
Heavy Atom Count:13
Complexity:195

Purity/Quality:

95% ^*data from raw suppliers

1,2,3,4-TETRAHYDRO-PYRAZINO[1,2-A]BENZIMIDAZOLE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN2C(=NC3=CC=CC=C32)CN1

Technology Process of 1,2,3,4-Tetrahydropyrazino[1,2-a]benzimidazole

There total 12 articles about 1,2,3,4-Tetrahydropyrazino[1,2-a]benzimidazole 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: 84.0%

: 245-49-8
benzo[4,5]imidazo[1,2-a]pyrazine

: 4744-53-0
NSC 700996

Guidance literature:: With hydrogen; palladium on activated charcoal; for 24h; under 2280 Torr;
DOI:10.3891/acta.chem.scand.51-0742

Reference yield: 73.0%

: 5805-57-2
2-Aminomethylbenzimidazole

: 106-93-4
ethylene dibromide

: 4744-53-0
NSC 700996

Guidance literature:: With sodium hydroxide; tetrabutylammomium bromide; In N,N-dimethyl-formamide; for 4h; Ambient temperature;

Reference yield: 50.4%

: 106-93-4
ethylene dibromide

: 7757-21-3
(1H-benzo[d]imidazol-2-yl)methanamine hydrochloride

: 4744-53-0
NSC 700996

Guidance literature:: (1H-benzo[d]imidazol-2-yl)methanamine hydrochloride; With tetrabutylammomium bromide; sodium hydroxide; at 25 ℃; for 1h;

ethylene dibromide; In N,N-dimethyl-formamide; at 25 ℃; for 4h;