N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine

Base Information

Chemical Name:N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine
CAS No.:827031-35-6
Molecular Formula:C16H16N4
Molecular Weight:264.33
Hs Code.:
ChEMBL ID:CHEMBL475381
DSSTox Substance ID:DTXSID70462015

Synonyms:827031-35-6;N1-METHYL-N1-(2-METHYLQUINAZOLIN-4-YL)BENZENE-1,4-DIAMINE;N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine;CHEMBL475381;SCHEMBL2256177;DTXSID70462015;VJPRMSSYQNPZGF-UHFFFAOYSA-N;(2-methyl-quinazolin-4-yl)-(4-amino-phenyl)-methylamine;(4-Amino-phenyl)-(2-methyl-quinazolin-4-yl)-methyl-amine;(4-amino-phenyl)-(2-methyl-quinazolin-4-yl)-methylamine

Suppliers and Price of N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine

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 2 raw suppliers

Chemical Property of N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:264.137496527
Heavy Atom Count:20
Complexity:314

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NC2=CC=CC=C2C(=N1)N(C)C3=CC=C(C=C3)N

Technology Process of N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine

There total 3 articles about N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine 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: 78.0%

: 2,N-dimethyl-N-(4-nitrophenyl)quinazolin-4-amine

: 827031-35-6
N-(4-aminophenyl)-N,2-dimethylquinazolin-4-amine

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; for 4h; under 2585.81 Torr;

Reference yield:

: 100-15-2
N-methyl(p-nitroaniline)

: 827031-35-6
N-(4-aminophenyl)-N,2-dimethylquinazolin-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1: isopropyl alcohol / 20 °C

2: 5%-palladium/activated carbon; hydrogen / methanol / 20 °C

With 5%-palladium/activated carbon; hydrogen; In methanol; isopropyl alcohol;
DOI:10.1111/cbdd.13405

Reference yield:

: 6484-24-8
2-methyl-4-chloroquinazoline

: 827031-35-6
N-(4-aminophenyl)-N,2-dimethylquinazolin-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1: isopropyl alcohol / 20 °C

2: 5%-palladium/activated carbon; hydrogen / methanol / 20 °C

With 5%-palladium/activated carbon; hydrogen; In methanol; isopropyl alcohol;
DOI:10.1111/cbdd.13405