1-Benzyl-1,2,3,4-tetrahydroquinoxaline

Base Information

Chemical Name:1-Benzyl-1,2,3,4-tetrahydroquinoxaline
CAS No.:2602-45-1
Molecular Formula:C15H16 N2
Molecular Weight:224.305
Hs Code.:2933990090
European Community (EC) Number:821-872-6
DSSTox Substance ID:DTXSID10585732
Nikkaji Number:J2.357.215J
Wikidata:Q82477718
Mol file:2602-45-1.mol

Synonyms:1-Benzyl-1,2,3,4-tetrahydroquinoxaline;2602-45-1;4-benzyl-2,3-dihydro-1H-quinoxaline;SCHEMBL6419724;DTXSID10585732;QDTKGICRPUUWCY-UHFFFAOYSA-N;CS-0221923;EN300-100617

Suppliers and Price of 1-Benzyl-1,2,3,4-tetrahydroquinoxaline

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
1-benzyl-1,2,3,4-tetrahydroquinoxaline
10mg
$ 45.00

American Custom Chemicals Corporation
1-BENZYL-1,2,3,4-TETRAHYDROQUINOXALINE 95.00%
5MG
$ 499.20

AK Scientific
1-Benzyl-1,2,3,4-tetrahydroquinoxaline
1g
$ 1107.00

AK Scientific
1-Benzyl-1,2,3,4-tetrahydroquinoxaline
500mg
$ 890.00

Total 5 raw suppliers

Chemical Property of 1-Benzyl-1,2,3,4-tetrahydroquinoxaline

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Refractive Index:1.61
Boiling Point:395.6°Cat760mmHg
PKA:6.69±0.20(Predicted)
Flash Point:184.1°C
PSA：15.27000
Density:1.112g/cm³
LogP:3.32170
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:224.131348519
Heavy Atom Count:17
Complexity:235

Purity/Quality:

99% ^*data from raw suppliers

1-benzyl-1,2,3,4-tetrahydroquinoxaline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(C2=CC=CC=C2N1)CC3=CC=CC=C3

Technology Process of 1-Benzyl-1,2,3,4-tetrahydroquinoxaline

There total 9 articles about 1-Benzyl-1,2,3,4-tetrahydroquinoxaline 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: 90.0%

: 106595-91-9
4-benzyl-3,4-dihydroquinoxalin-2(1H)-one

: 2602-45-1
1-benzyl-1,2,3,4-tetrahydroquinoxaline

Guidance literature:: With [RuCl₂(N-heterocyclic carbene)(bis[2-(diphenylphosphino)ethyl]amine)]; hydrogen; caesium carbonate; In toluene; butan-1-ol; at 150 ℃; for 6h; under 22502.3 Torr; Schlenk technique; Autoclave;
DOI:10.1021/acs.orglett.9b03878

Reference yield: 19.0%

: 912284-71-0
2-[(2-aminophenyl)(benzyl)amino]ethan-1-ol

: 2602-45-1
1-benzyl-1,2,3,4-tetrahydroquinoxaline

Guidance literature:: With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; potassium carbonate; In toluene; at 120 ℃; for 96h;
DOI:10.1016/j.tetlet.2006.07.033

Reference yield:

: 2-[benzyl(2-nitrophenyl)amino]ethan-1-ol

: 2602-45-1
1-benzyl-1,2,3,4-tetrahydroquinoxaline

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd/C

2: 19 percent / K₂CO₃; [Cp*IrCl₂]2 / toluene / 96 h / 120 °C

With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; hydrogen; potassium carbonate; palladium on activated charcoal; In toluene;
DOI:10.1016/j.tetlet.2006.07.033