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N-Nitrosodihydrodibenzazepine

Base Information
  • Chemical Name:N-Nitrosodihydrodibenzazepine
  • CAS No.:7458-08-4
  • Molecular Formula:C14H12 N2 O
  • Molecular Weight:224.262
  • Hs Code.:
  • European Community (EC) Number:231-232-2
  • DSSTox Substance ID:DTXSID90996089
  • Nikkaji Number:J278.858F
  • Wikidata:Q82987748
  • Mol file:7458-08-4.mol
N-Nitrosodihydrodibenzazepine

Synonyms:N-NDHDBA;N-nitroso-10,11-dihydro-5H-dibenz(b,f)azepine;N-nitrosodihydrodibenzazepine;N-nitrosoiminodibenzyl

Suppliers and Price of N-Nitrosodihydrodibenzazepine
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
  • N-NITROSODIHYDRODIBENZAZEPINE 95.00%
  • 5MG
  • $ 503.72
Total 7 raw suppliers
Chemical Property of N-Nitrosodihydrodibenzazepine
Chemical Property:
  • Vapor Pressure:4.44E-06mmHg at 25°C 
  • Boiling Point:383.3°C at 760 mmHg 
  • Flash Point:185.6°C 
  • PSA:32.67000 
  • Density:1.21g/cm3 
  • LogP:3.66970 
  • Storage Temp.:-20°C Freezer, Under inert atmosphere 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly) 
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:224.094963011
  • Heavy Atom Count:17
  • Complexity:257
Purity/Quality:

99% *data from raw suppliers

N-NITROSODIHYDRODIBENZAZEPINE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CC2=CC=CC=C2N(C3=CC=CC=C31)N=O
  • Uses N-Nitrosoiminodibenzyl is an N-nitroso derivative of 10,11-Dihydro-5H-dibenzo[b,f]azepine (D448870), which is a metabolite of the tricyclic antidepressant, Imipramine (I465980). 10,11-Dihydro-5H-dibenzo[b,f]azepine can be used as a chromogenic probe for the quantification of hydrogen peroxide and glucose. N-Nitrosoiminodibenzyl can be used as antidepressives and antiepileptics.
Technology Process of N-Nitrosodihydrodibenzazepine

There total 4 articles about N-Nitrosodihydrodibenzazepine 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:
Guidance literature:
9,10-dihydrodibenzazepine; With hydrogenchloride; In water; acetonitrile; at 0 ℃;
With sodium nitrite; In water; acetonitrile;
DOI:10.1021/ol402523x
Guidance literature:
With 4-(1,1-dimethylethyl)benzoic acid; In dichloromethane; at 20 ℃; for 24h; Inert atmosphere; Glovebox; Schlenk technique;
DOI:10.1039/c9cc04529e
Guidance literature:
With diethyl ether; acetic acid; sodium nitrite;
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