3-Amino-4-methyl-4,6,7,8-tetrahydroquinoxaline-2-carbonitrile

Base Information

Chemical Name:3-Amino-4-methyl-4,6,7,8-tetrahydroquinoxaline-2-carbonitrile
CAS No.:107938-84-1
Molecular Formula:C₁₀H₁₂N₄
Molecular Weight:188.232
Hs Code.:
DSSTox Substance ID:DTXSID90545632
Wikidata:Q82423189
Mol file:107938-84-1.mol

Synonyms:107938-84-1;3-AMINO-4-METHYL-4,6,7,8-TETRAHYDROQUINOXALINE-2-CARBONITRILE;3-AMINO-4-METHYL-7,8-DIHYDRO-6H-QUINOXALINE-2-CARBONITRILE;2-Quinoxalinecarbonitrile,3-amino-4,6,7,8-tetrahydro-4-methyl-(9CI);DTXSID90545632

Suppliers and Price of 3-Amino-4-methyl-4,6,7,8-tetrahydroquinoxaline-2-carbonitrile

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

AccelPharmtech
3-amino-4,6,7,8-tetrahydro-4-methyl-2-Quinoxalinecarbonitrile 97.00%
25G
$ 6000.00

AccelPharmtech
3-amino-4,6,7,8-tetrahydro-4-methyl-2-Quinoxalinecarbonitrile 97.00%
5G
$ 3230.00

AccelPharmtech
3-amino-4,6,7,8-tetrahydro-4-methyl-2-Quinoxalinecarbonitrile 97.00%
1G
$ 1890.00

Total 1 raw suppliers

Chemical Property of 3-Amino-4-methyl-4,6,7,8-tetrahydroquinoxaline-2-carbonitrile

Chemical Property:

Melting Point:158 °C(Solv: ethanol (64-17-5))
Boiling Point:352.0±42.0 °C(Predicted)
PKA:10.07±0.40(Predicted)
PSA：67.63000
Density:1.30±0.1 g/cm3(Predicted)
LogP:0.85308
XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:188.106196400
Heavy Atom Count:14
Complexity:405

Purity/Quality:: 3-amino-4,6,7,8-tetrahydro-4-methyl-2-Quinoxalinecarbonitrile 97.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2=CCCCC2=NC(=C1N)C#N

Technology Process of 3-Amino-4-methyl-4,6,7,8-tetrahydroquinoxaline-2-carbonitrile

There total 1 articles about 3-Amino-4-methyl-4,6,7,8-tetrahydroquinoxaline-2-carbonitrile 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: 69.0%

: 74-89-5
methylamine

: 49845-13-8
(morpholino-2-cyclohexene-1-ylimino)malononitrile

: 107938-84-1
amino-2-methyl-1-tetrahydro-1,5,6,7-quinoxalinecarbonitrile-3

Guidance literature:: In methanol; chloroform; for 12h; Ambient temperature;
DOI:10.1002/hlca.19860690510

Reference yield: 55.0%

: 103-71-9
phenyl isocyanate

: 107938-84-1
amino-2-methyl-1-tetrahydro-1,5,6,7-quinoxalinecarbonitrile-3

: 117286-19-8
methyl-1-(phenylcarbamoyl)imino-2-hexahydro-1,2,5,6,7,8-quinoxalinecarbonitrile-3

Guidance literature:: In chloroform; at 20 ℃; for 24h;

Reference yield:

: 107938-84-1
amino-2-methyl-1-tetrahydro-1,5,6,7-quinoxalinecarbonitrile-3

: 117286-27-8
amino-4-methyl-10-phenyl-3-tetrahydro-6,7,8,10-benzopteridinone-2

Guidance literature:: Multi-step reaction with 2 steps

1: 55 percent / CHCl₃ / 24 h / 20 °C

2: 71 percent / triethyl amine / methanol / 0.33 h / Heating

With triethylamine; In methanol; chloroform;