109423-08-7

Basic information

• Product Name: 1,3,5-Triazine, hexahydro-1,3,5-tris(3-methylphenyl)-
• CAS NO: 109423-08-7
• Molecular Formula: C24H27N3
• Molecular Weight: 357.498
• Mol File: 109423-08-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,3,5-Triazine, hexahydro-1,3,5-tris(3-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Triazine, hexahydro-1,3,5-tris(3-methylphenyl)-(109423-08-7)
• EPA Substance Registry System: 1,3,5-Triazine, hexahydro-1,3,5-tris(3-methylphenyl)-(109423-08-7)

Safety Data

• Hazardous Substances Data: 109423-08-7(Hazardous Substances Data)

Upstream product

• 88919-93-1 3-toluidine 
• 50-00-0 formaldehyd 
• 108-44-1 1-amino-3-methylbenzene 
• 229323-97-1 2,2-dihydroperoxyadamantane 

Downstream Products

• 3551-75-5 N,N'-bis(3-methylphenyl)oxalamide 
• 109423-13-4 Trifluoro-acetic acid [m-tolyl-(2,2,2-trifluoro-acetyl)-amino]-methyl ester 
• 41977-54-2 (Z)-3-methylbenzaldehyde oxime 
• 41977-54-2 3-methyl-benzaldehyde (E)-oxime 

Relevant articles and documents

Synthesis, molecular structure, conformation and biological activity of Ad-substituted N-aryl-tetraoxaspiroalkanes

An efficient method has been developed for the synthesis of 7′-arylspiro{adamantane-[2,3′]-(1′,2′,4′,5′,7′-tetraoxazocanes)} by the ring transformation reaction of spiro{adamantane-[2,3’]-(1′,2′,4′,5′,7′-pentaoxacane)} with arylamines in the presence of S

Facile Access to 3-Unsubstituted Tetrahydroisoquinolonic Acids via the Castagnoli-Cushman Reaction

Hitherto undescribed 3-unsubstituted tetrahydroisoquinolonic acids (isolated as their respective methyl esters) were accessed for the first time by the uncatalyzed, thermally promoted Castagnoli-Cushman reaction (CCR) of homophthalic anhydride (HPA) and a series of 1,3,5-triazinanes. The moderate yields observed in some cases are most likely associated with a persistent impurity also formed in these reactions. The new scaffold is expected to find novel medicinal utility (compared to the traditional CCR adducts) because it lacks a substituent at the 3-position.

Novel oxidative nitrogen to carbon rearrangement found in the conversion of anilines to benzaldoximes by treating with HCHO/H2O2

Novel rearrangement was found by reacting anilines with HCHO/H2O2 resulting in the synthesis of various benzaldoximes. The mechanism of the rearrangement is proposed and suggested that the rearrangement might proceed via unstable N-phenyloxazirane intermediate followed by the transfer of aryl moiety from nitrogen to carbon atom leading to the formation of benzaldoxime.