CAS 959-52-4

1,1′,1′′-(1,3,5-Triazine-1,3,5(2H,4H,6H)-triyl)tris[2-propen-1-one]

Description:

1,1′,1′′-(1,3,5-Triazine-1,3,5(2H,4H,6H)-triyl)tris[2-propen-1-one], commonly referred to as a triazine derivative, is a chemical compound characterized by its triazine core structure, which consists of a six-membered ring containing three nitrogen atoms. This compound features three 2-propen-1-one (acrylonitrile) groups attached to the triazine ring, contributing to its reactivity and potential applications in various fields, including materials science and organic synthesis. The presence of multiple reactive double bonds in the 2-propen-1-one moieties allows for polymerization and cross-linking reactions, making it useful in the development of polymers and resins. Additionally, the triazine structure can impart unique electronic properties, which may enhance its utility in electronic materials or as a ligand in coordination chemistry. The compound is typically synthesized through multi-step organic reactions and may exhibit interesting photophysical properties, making it a subject of interest in research related to photochemistry and photophysics. Safety data should be consulted for handling and usage, as with all chemical substances.

Formula: C₁₂H₁₅N₃O₃

InChI: InChI=1S/C12H15N3O3/c1-4-10(16)13-7-14(11(17)5-2)9-15(8-13)12(18)6-3/h4-6H,1-3,7-9H2

InChI key: InChIKey=FYBFGAFWCBMEDG-UHFFFAOYSA-N

SMILES: C(C=C)(=O)N1CN(C(C=C)=O)CN(C(C=C)=O)C1

Synonyms:

• 1,1',1''-(1,3,5-Triazinane-1,3,5-Triyl)Trisprop-2-En-1-One
• 1,1′,1′′-(1,3,5-Triazine-1,3,5(2H,4H,6H)-triyl)tris[2-propen-1-one]
• 1,3,5-Triacryloyl-hexahydro-s-triazine
• 1,3,5-Triacryloyl-s-triazine
• 1,3,5-Triacryloylaminohexahydro-s-triazine
• 1,3,5-Triacryloylhexahydro-s-triazine
• 1,3,5-Triacryloylhexahydrotriazine
• 1,3,5-Triacryloyltrimethylenetriamine
• 1,3,5-Triazine, hexahydro-1,3,5-tris(1-oxo-2-propenyl)-
• 1,3,5-Tris(acryloyl)hexahydro-s-triazine
• 1-[3,5-Di(prop-2-enoyl)-1,3,5-triazinan-1-yl]prop-2-en-1-one
• 2-Propen-1-one, 1,1′,1′′-(1,3,5-triazine-1,3,5(2H,4H,6H)-triyl)tris-
• Du 801
• Fixierer P
• Fixing Agent P
• Hexahydro-1,3,5-triacryloyl-s-triazine
• Hexahydrotris(acryloyl)-s-triazine
• NSC 63839
• NSC 8185
• TAF (crosslinking agent)
• Tri(N-acryloyl)hexahydrotriazine
• Triacrylformal
• Triacryloylhexahydro-s-triazine
• Triacryloylhexahydrotriazine
• Triacryloylperhydrotriazine
• Tris(N-acryloyl)hexahydrotriazine
• Tris(acryloyl)hexahydro-s-triazine

1,3,5-Triacryloylhexahydro-1,3,5-triazine

CAS: 959-52-4

1,3,5-Triacryloylhexahydro-1,3,5-triazine

Formula: C₁₂H₁₅N₃O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 249.27

Ref: 54-OR80680

1,3,5-Triacryloylhexahydro-1,3,5-triazine

CAS: 959-52-4

Formula: C₁₂H₁₅N₃O₃

Purity: >98.0%(HPLC)(N)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 249.27

Ref: 3B-T1000

1-[3,5-Bis(prop-2-enoyl)-1,3,5-triazinan-1-yl]prop-2-en-1-one

CAS: 959-52-4

Formula: C₁₂H₁₅N₃O₃

Purity: 98%

Color and Shape: Solid, No data available.

Molecular weight: 249.27

Ref: 10-F181565

1,3,5-Triacryloylhexahydro-1,3,5-triazine

CAS: 959-52-4

1,3,5-Triacryloylhexahydro-1,3,5-triazine (TTH) is a particle that absorbs UV light. It is a reactive chemical with a high thermal stability and low reactivity to air. TTH has been used as a cross-linker in polymer films and as a microsphere filler. The absorption of UV light by TTH may be due to the presence of hydroxyl groups or nitrogen atoms. The nmr spectra show that TTH contains trimethylolpropane groups.

Formula: C₁₂H₁₅N₃O₃

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 249.27 g/mol

Ref: 3D-FT29992