2-(4-Chlorophenyl)-4,6-dimethyl-1,3,5-triazine

Base Information

Chemical Name:2-(4-Chlorophenyl)-4,6-dimethyl-1,3,5-triazine
CAS No.:30362-08-4
Molecular Formula:C11H10 Cl N3
Molecular Weight:219.6702
Hs Code.:
DSSTox Substance ID:DTXSID60275232
Nikkaji Number:J1.613.694H
Wikidata:Q82004911
Mol file:30362-08-4.mol

Synonyms:30362-08-4;2-(4-chlorophenyl)-4,6-dimethyl-1,3,5-triazine;SCHEMBL16117348;DTXSID60275232;2-(4-Chlorophenyl)-4,6-dimethyl-s-triazine

Suppliers and Price of 2-(4-Chlorophenyl)-4,6-dimethyl-1,3,5-triazine

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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Total 0 raw suppliers

Chemical Property of 2-(4-Chlorophenyl)-4,6-dimethyl-1,3,5-triazine

Chemical Property:

Vapor Pressure:1.6E-06mmHg at 25°C
Boiling Point:408.9°Cat760mmHg
Flash Point:233.5°C
Density:1.227g/cm³
XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:219.0563250
Heavy Atom Count:15
Complexity:194

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NC(=NC(=N1)C2=CC=C(C=C2)Cl)C

Technology Process of 2-(4-Chlorophenyl)-4,6-dimethyl-1,3,5-triazine

There total 4 articles about 2-(4-Chlorophenyl)-4,6-dimethyl-1,3,5-triazine 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: 76.0%

: 124-42-5
acetamidine hydrochloride

: 104-88-1
4-chlorobenzaldehyde

: 30362-08-4
2-(4-chlorophenyl)-4,6-dimethyl-1,3,5-triazine

Guidance literature:: With caesium carbonate; In dimethyl sulfoxide; at 90 ℃; for 12h; Inert atmosphere;
DOI:10.1002/ejoc.201200276

Reference yield: 62.0%

: 124-42-5
acetamidine hydrochloride

: 83253-09-2
4-Chloro-N-[1-ethylsulfanyl-eth-(Z)-ylidene]-benzamide

: 30362-08-4
2-(4-chlorophenyl)-4,6-dimethyl-1,3,5-triazine

Guidance literature:: With sodium methylate; In ethanol; Ambient temperature;

Reference yield:

: 2905-48-8
N-thioacetyl-4-chlorobenzamide

: 30362-08-4
2-(4-chlorophenyl)-4,6-dimethyl-1,3,5-triazine

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / K₂CO₃ / acetonitrile / 60 °C

2: 62 percent / Sodium methoxide / ethanol / Ambient temperature

With sodium methylate; potassium carbonate; In ethanol; acetonitrile;