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

Base Information

• Chemical Name: 2,4,6-Triethylhexahydro-1,3,5-triazine
• CAS No.: 102-26-1
• Molecular Formula: C9H21 N3
• Molecular Weight: 171.286
• Hs Code.: 2933699090
• European Community (EC) Number: 203-018-9
• UNII: WAB39D2LKD
• DSSTox Substance ID: DTXSID80144512
• Nikkaji Number: J182.153I
• Mol file: 102-26-1.mol

Synonyms:2,4,6-triethyl-1,3,5-triazinane;102-26-1;2,4,6-Triethylhexahydro-1,3,5-triazine;EINECS 203-018-9;1,3,5-Triazine, 2,4,6-triethylhexahydro-;2,4,6-triethyl-[1,3,5]triazinane;WAB39D2LKD;SCHEMBL13889209;DTXSID80144512;s-Triazine, 2,4,6-triethylhexahydro-;2,4,6-triethylhexahydro-1,3,5-triazin

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

Chemical Property:

• Vapor Pressure: 0.553mmHg at 25°C
• Boiling Point: 190°Cat760mmHg
• Flash Point: 56.6°C
• PSA: 36.09000
• Density: 0.826g/cm³
• LogP: 1.96350
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 171.173547683
• Heavy Atom Count: 12
• Complexity: 91.2

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1NC(NC(N1)CC)CC

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

There total 6 articles about 2,4,6-Triethylhexahydro-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: 55.0%

propionaldehyde (123-38-6) → 2,4,6-triethyl-1,3,5-hexahydrotriazine (102-26-1)

Guidance literature:

With ammonia; In acetonitrile; for 15h;

Reference yield:

C16H15NO (104410-31-3) → 2,4,6-triethyl-1,3,5-hexahydrotriazine (102-26-1) + 9-fluorenone (486-25-9,952573-42-1)

Guidance literature:

With 1,4-diaza-bicyclo[2.2.2]octane; chloroform-d1; Yield given;

Reference yield:

C16H15NO (104410-31-3) → 2,4,6-triethyl-1,3,5-hexahydrotriazine (102-26-1) + 9-fluorenone (486-25-9,952573-42-1) + C9H18N2 (40899-13-6) + propionaldehyde (123-38-6)

Guidance literature:

Yield given. Yields of byproduct given; Ambient temperature; 2-3 days;

upstream raw materials:

propan-1-imine

C₁₆H₁₅NO

propionaldehyde

Cyclopropylamine

Downstream raw materials:

propionaldehyde

Refernces

• 1、 Crampton, Michael R.,Lord, Simon D.,Millar, Ross. "Some reactions of ammonia and primary amines with propanal, 2-chloroethanal, 2,2-dichloroethanal and 2,2,2-trichloroethanal in acetonitrile". . p. 909 - 914. Retrieved 2007/10/03.
• 2、 Boyd, Derek R.,Coulter, Peter B.,Hamilton, Robert,Thompson, Norris T.,Sharma, Narain D.,Stubbs, Michael E.. "The Synthesis of NH Aldimines and Derivatives by Spontaneous and Base-catalysed Decomposition of Oxaziridines". . p. 2123 - 2128. Retrieved 2007/10/02.