(1E)-1-(2-Methoxyphenyl)-3,3-dimethyltriaz-1-ene

Base Information

Chemical Name:(1E)-1-(2-Methoxyphenyl)-3,3-dimethyltriaz-1-ene
CAS No.:20240-99-7
Molecular Formula:C9H13N3O
Molecular Weight:179.222
Hs Code.:
NSC Number:173097
DSSTox Substance ID:DTXSID10305992
Nikkaji Number:J1.605.778I
ChEMBL ID:CHEMBL3250817

Synonyms:20240-99-7;NSC173097;CHEMBL3250817;DTXSID10305992;NSC-173097;(1E)-1-(2-Methoxyphenyl)-3,3-dimethyltriaz-1-ene

Suppliers and Price of (1E)-1-(2-Methoxyphenyl)-3,3-dimethyltriaz-1-ene

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 (1E)-1-(2-Methoxyphenyl)-3,3-dimethyltriaz-1-ene

Chemical Property:

Vapor Pressure:0.0102mmHg at 25°C
Boiling Point:263.6°Cat760mmHg
Flash Point:113.2°C
Density:1.03g/cm³
XLogP3:2.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:179.105862047
Heavy Atom Count:13
Complexity:170

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)N=NC1=CC=CC=C1OC

Technology Process of (1E)-1-(2-Methoxyphenyl)-3,3-dimethyltriaz-1-ene

There total 3 articles about (1E)-1-(2-Methoxyphenyl)-3,3-dimethyltriaz-1-ene 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:

: 90-04-0
2-methoxy-phenylamine

: 124-40-3
dimethyl amine

: 20240-99-7
1-(2-Methoxyphenyl)-3,3-dimethyltriazen

Guidance literature:: With hydrogenchloride; sodium carbonate; sodium nitrite; Yield given. Multistep reaction; 2.) 30 min;
DOI:10.1002/ardp.19813140711