3,3'-Dimethoxyazobenzene

Base Information

Chemical Name:3,3'-Dimethoxyazobenzene
CAS No.:6319-23-9
Molecular Formula:C14H14N2O2
Molecular Weight:242.277
Hs Code.:
NSC Number:31010
Nikkaji Number:J1.027.668C

Synonyms:3,3'-DIMETHOXYAZOBENZENE;NSC 31010;6319-23-9;NSC31010;SCHEMBL10818541;SCHEMBL17707284;NSC-31010

Suppliers and Price of 3,3'-Dimethoxyazobenzene

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 6 raw suppliers

Chemical Property of 3,3'-Dimethoxyazobenzene

Chemical Property:

Vapor Pressure:4.56E-06mmHg at 25°C
Boiling Point:394.3°C at 760 mmHg
Flash Point:155.5°C
Density:1.09g/cm³
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:242.105527694
Heavy Atom Count:18
Complexity:245

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=CC(=C1)N=NC2=CC(=CC=C2)OC

Technology Process of 3,3'-Dimethoxyazobenzene

There total 18 articles about 3,3'-Dimethoxyazobenzene 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: 97.0%

: 536-90-3,918666-97-4
m-Anisidine

: 6319-23-9
1,2-bis(3-methoxyphenyl)diazene

Guidance literature:: With copper-manganese spinel oxide; In ethyl acetate; at 80 ℃; for 5h;
DOI:10.1002/cctc.201501218

Reference yield: 95.0%

: 555-03-3
3-nitroanisole

: 6319-23-9
1,2-bis(3-methoxyphenyl)diazene

Guidance literature:: With chloro-trimethyl-silane; samarium diiodide; tetra-(n-butyl)ammonium iodide; tert-butylammonium hexafluorophosphate(V); In tetrahydrofuran; at 20 ℃; for 5h; Electrochemical reaction;
DOI:10.1021/acscatal.7b02940