53888-70-3

Basic information

• Product Name: 1-(2-Propenyl)-3,5-bis[3-(tributylstannyl)propyl]-1,3,5-triazine-2,4,6(1H,3H,5H)-trione
• Synonyms: 1-(2-Propenyl)-3,5-bis[3-(tributylstannyl)propyl]-1,3,5-triazine-2,4,6(1H,3H,5H)-trione
• CAS NO: 53888-70-3
• Molecular Formula: C36H71N3O3Sn2
• Molecular Weight: 831.38724
• Mol File: 53888-70-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(2-Propenyl)-3,5-bis[3-(tributylstannyl)propyl]-1,3,5-triazine-2,4,6(1H,3H,5H)-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-Propenyl)-3,5-bis[3-(tributylstannyl)propyl]-1,3,5-triazine-2,4,6(1H,3H,5H)-trione(53888-70-3)
• EPA Substance Registry System: 1-(2-Propenyl)-3,5-bis[3-(tributylstannyl)propyl]-1,3,5-triazine-2,4,6(1H,3H,5H)-trione(53888-70-3)

Safety Data

• Hazardous Substances Data: 53888-70-3(Hazardous Substances Data)

Usage

Chemical Family

Belongs to the triazine-2,4,6(1H,3H,5H)-trione family, which is a group of organic compounds containing a triazine ring with three carbonyl groups attached.

Structure

Contains a triazine ring with multiple propenyl and tributylstannyl groups attached. The triazine ring is a six-membered ring with alternating nitrogen and carbon atoms.

Propenyl Groups

The compound has propenyl groups (C3H5) attached to the triazine ring. These groups consist of a vinyl group (C2H3) attached to a methyl group (CH3), providing a source of unsaturation and reactivity.

Tributylstannyl Groups

The compound features tributylstannyl groups (C12H27Sn) attached to the propyl groups. These groups consist of a tin atom bonded to three butyl groups (C4H9), which can provide steric bulk and organometallic reactivity.

Potential Applications

Has potential applications in organic synthesis and materials science due to its ability to undergo various reactions and form new compounds.

Building Block

Can be used as a building block for the synthesis of more complex organic molecules, such as polymers, pharmaceuticals, and other specialty chemicals.

Organometallic Chemistry

The presence of the tributylstannyl group makes the compound useful in organometallic chemistry for the introduction of this group into other organic molecules, which can be important for the development of new materials and catalysts.

Reactivity

The compound's reactivity can be attributed to the presence of the propenyl and tributylstannyl groups, which can participate in various chemical reactions, such as cross-coupling, substitution, and addition reactions.

Stereoisomers

Due to the presence of multiple chiral centers, the compound may exist as a mixture of stereoisomers, which can have different properties and reactivities.

Solubility

The compound is likely to be soluble in organic solvents, such as chloroform, dichloromethane, and tetrahydrofuran, due to its nonpolar nature and the presence of the tributylstannyl groups.