4-(4-nitrophenyl)-2,3-dihydro-1H-1,5-benzodiazepine

Base Information

Chemical Name:4-(4-nitrophenyl)-2,3-dihydro-1H-1,5-benzodiazepine
CAS No.:283610-70-8
Molecular Formula:C₁₅H₁₃N₃O₂
Molecular Weight:267.287
Hs Code.:
DSSTox Substance ID:DTXSID80378032
Nikkaji Number:J1.316.929B
Mol file:283610-70-8.mol

Synonyms:283610-70-8;4-(4-nitrophenyl)-2,3-dihydro-1H-1,5-benzodiazepine;1H-1,5-Benzodiazepine,2,3-dihydro-4-(4-nitrophenyl)-;4-(4-Nitro-phenyl)-2,3-dihydro-1H-benzo[b][1,4]diazepine;MFCD06245404;DTXSID80378032;AKOS005254260;2,3-Dihydro-4-(4-nitrophenyl)-1H-1,5-benzodiazepine;4-(4-Nitrophenyl)-2,3-dihydro-1H-benzo[b][1,4]diazepine;(E)-4-(4-nitrophenyl)-2,3-dihydro-1H-benzo[b][1,4]diazepine

Suppliers and Price of 4-(4-nitrophenyl)-2,3-dihydro-1H-1,5-benzodiazepine

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
4-(4-NITRO-PHENYL)-2,3-DIHYDRO-1H-BENZO[B][1,4]DIAZEPINE 95.00%
50MG
$ 714.29

Total 6 raw suppliers

Chemical Property of 4-(4-nitrophenyl)-2,3-dihydro-1H-1,5-benzodiazepine

Chemical Property:

Vapor Pressure:2.91E-08mmHg at 25°C
Refractive Index:1.668
Boiling Point:449.2°Cat760mmHg
Flash Point:225.5°C
Density:1.31g/cm³
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:267.100776666
Heavy Atom Count:20
Complexity:383

Purity/Quality:

97% ^*data from raw suppliers

4-(4-NITRO-PHENYL)-2,3-DIHYDRO-1H-BENZO[B][1,4]DIAZEPINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CNC2=CC=CC=C2N=C1C3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of 4-(4-nitrophenyl)-2,3-dihydro-1H-1,5-benzodiazepine

There total 1 articles about 4-(4-nitrophenyl)-2,3-dihydro-1H-1,5-benzodiazepine 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: 60.0%