Carbamic acid, (4-(9-acridinylamino)phenyl)-, methyl ester

Base Information

Chemical Name:Carbamic acid, (4-(9-acridinylamino)phenyl)-, methyl ester
CAS No.:64990-16-5
Molecular Formula:C₂₁H₁₇N₃O₂
Molecular Weight:343.385
Hs Code.:
DSSTox Substance ID:DTXSID20215311
Nikkaji Number:J458.732D
Wikidata:Q83091322
ChEMBL ID:CHEMBL278384

Synonyms:64990-16-5;Carbamic acid, (4-(9-acridinylamino)phenyl)-, methyl ester;4-(9-Acridinylamino)phenylcarbamic acid, methyl ester;Methyl (4-(9-acridinylamino)phenyl)carbamate;CHEMBL278384;DTXSID20215311;methyl N-(4-(9-acridinylamino)-phenyl)carbamate

Suppliers and Price of Carbamic acid, (4-(9-acridinylamino)phenyl)-, methyl ester

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
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price

Total 1 raw suppliers

Chemical Property of Carbamic acid, (4-(9-acridinylamino)phenyl)-, methyl ester

Chemical Property:

Vapor Pressure:1.46E-09mmHg at 25°C
Boiling Point:485.1°C at 760 mmHg
Flash Point:247.2°C
Density:1.339g/cm³
XLogP3:4.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:343.132076794
Heavy Atom Count:26
Complexity:456

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

Safty Information:

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MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)NC1=CC=C(C=C1)NC2=C3C=CC=CC3=NC4=CC=CC=C42

Technology Process of Carbamic acid, (4-(9-acridinylamino)phenyl)-, methyl ester

There total 1 articles about Carbamic acid, (4-(9-acridinylamino)phenyl)-, methyl ester 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: