2,4,6-trimethyl-1,3,5-triazine

Base Information

• Chemical Name: 2,4,6-trimethyl-1,3,5-triazine
• CAS No.: 823-94-9
• Molecular Formula: C6H9N3
• Molecular Weight: 123.158
• Mol file: 823-94-9.mol

Synonyms:2,4,6-trimethyl-s-triazine;s-Triazine,2,4,6-trimethyl;2,4,6-trimethyl-[1,3,5]triazine;1,3,5-Triazine,2,4,6-trimethyl;2,4,6-tris(methyl)-s-triazine;1,3,5-trimethyl-s-triazine;3,4,6-trimethyl-1,3,5-triazine;2,4,6-trimethyl-1,3,5-s-triazine;

Chemical Property of 2,4,6-trimethyl-1,3,5-triazine

Chemical Property:

• Vapor Pressure: 0.00386mmHg at 25°C
• Melting Point: 59-60 °C
• Boiling Point: 289.3°Cat760mmHg
• PKA: 3.41±0.10(Predicted)
• Flash Point: 137°C
• PSA: 38.67000
• Density: 1.044g/cm³
• LogP: 0.79680
• Storage Temp.: Sealed in dry,Room Temperature

Purity/Quality:

99%, ^*data from raw suppliers

2,4,6-Trimethyl-1,3,5-triazine 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2,4,6-trimethyl-1,3,5-triazine

There total 16 articles about 2,4,6-trimethyl-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: 73.0%

acetonitrile (75-05-8,26809-02-9) → 2,4,6-trimethyl-s-triazine (823-94-9) + 4-amino-2,6-dimethylpyrimidine (461-98-3)

Guidance literature:

With ammonia; yttrium(III) trifluoromethanesulfonate; at -196 - 200 ℃; for 24h;

Reference yield: 73.0%

ammonia (7664-41-7) + acetonitrile (75-05-8,26809-02-9) → 2,4,6-trimethyl-s-triazine (823-94-9) + 4-amino-2,6-dimethylpyrimidine (461-98-3)

Guidance literature:

With yttrium(III) trifluoromethanesulfonate; at -196 - 200 ℃; for 24h;

Reference yield: 73.0%

→ 2,4,6-trimethyl-s-triazine (823-94-9) + 4-amino-2,6-dimethylpyrimidine (461-98-3)

Guidance literature:

upstream raw materials:

methanol

formamidine hydrochloride

acetamidine

acetonitrile

Downstream raw materials:

2,4-dimethyl-6-propyl-s-triazine

2,4-dimethyl-6-(2-methylpropyl)-s-triazine

2-Brommethyl-4,6-dimethyl-s-triazin

2,4,6-tris[(E)-2-{4-[(diethoxyphosphoryl)methyl]phenyl}ethenyl]-1,3,5-triazine

Refernces

• 1、 Salnikov, George E.,Genaev, Alexander M.,Vasiliev, Vladimir G.,Shubin, Vyacheslav G.. "Interaction of acetonitrile with trifluoromethanesulfonic acid: Unexpected formation of a wide variety of structures". supporting information; experimental part. p. 2282 - 2288. Retrieved 2012/04/10.
• 2、 -. "N-Fluorotriazinium fluorinating agents". Example 4. . Retrieved 2008/06/13.