C07C49/653

Oxocarbon-, pseudooxocarbon- and radialene compounds and their use

The present invention relates to oxocarbon-, pseudooxocarbon- and radialene compounds as well as to their use as doping agent for doping an organic semiconductive matrix material, as blocker material, as charge injection layer, as electrode material as well as organic semiconductor, as well as electronic components and organic semiconductive materials using them.

Oxocarbon-, pseudooxocarbon- and radialene compounds and their use

The present invention relates to oxocarbon-, pseudooxocarbon- and radialene compounds as well as to their use as doping agent for doping an organic semiconductive matrix material, as blocker material, as charge injection layer, as electrode material as well as organic semiconductor, as well as electronic components and organic semiconductive materials using them.

COMPOSITIONS OF OXYGENATED AMINES AND QUINONE METHIDES AS ANTIFOULANTS FOR VINYLIC MONOMERS
20200017656 · 2020-01-16 ·

Described are compositions and methods for inhibiting polymerization of a monomer (e.g., styrene) composition a quinone methide polymerization retarder and an oxygen-containing amine compound that is a tertiary amine or hydroxylamine. In a mixture, the oxygen-containing amine compound improves the efficacy of the quinone methide polymerization retarder and provides greater antipolymerant activity. In turn, the mixture reduces or prevents apparatus fouling and improves the purity of monomer streams.

BICYCLIC AROMA CHEMICALS
20240051905 · 2024-02-15 ·

The present invention relates to new bicyclic compounds as aroma chemicals. Specifically, it relates to the use of bicyclic aroma compounds as an aroma chemical and also for enhancing and/or modifying the aroma of a composition.

BICYCLIC AROMA CHEMICALS
20240051905 · 2024-02-15 ·

The present invention relates to new bicyclic compounds as aroma chemicals. Specifically, it relates to the use of bicyclic aroma compounds as an aroma chemical and also for enhancing and/or modifying the aroma of a composition.

Reaction sequence for the synthesis of nootkatone, dihydronootkatone, and tetrahydronootkatone

An inexpensive, stereoselective synthesis for nootkatone, tetrahydronootkatone, and their derivatives is disclosed utilizing ozonolysis. The starting materials used in the synthesis are inexpensive and the reactions are commercially feasible and amenable to scaling up. The principal starting material, ()--Pinene, is on the GRAS list (generally recognized as safe).

Reaction sequence for the synthesis of nootkatone, dihydronootkatone, and tetrahydronootkatone

An inexpensive, stereoselective synthesis for nootkatone, tetrahydronootkatone, and their derivatives is disclosed utilizing ozonolysis. The starting materials used in the synthesis are inexpensive and the reactions are commercially feasible and amenable to scaling up. The principal starting material, ()--Pinene, is on the GRAS list (generally recognized as safe).

REACTION SEQUENCE FOR THE SYNTHESIS OF NOOTKATONE, DIHYDRONOOTKATONE, AND TETRAHYDRONOOTKATONE

An inexpensive, stereoselective synthesis for nootkatone, tetrahydronootkatone, and their derivatives is disclosed utilizing ozonolysis. The starting materials used in the synthesis are inexpensive and the reactions are commercially feasible and amenable to scaling up. The principal starting material, ()--Pinene, is on the GRAS list (generally recognized as safe).

REACTION SEQUENCE FOR THE SYNTHESIS OF NOOTKATONE, DIHYDRONOOTKATONE, AND TETRAHYDRONOOTKATONE

An inexpensive, stereoselective synthesis for nootkatone, tetrahydronootkatone, and their derivatives is disclosed utilizing ozonolysis. The starting materials used in the synthesis are inexpensive and the reactions are commercially feasible and amenable to scaling up. The principal starting material, ()--Pinene, is on the GRAS list (generally recognized as safe).

BI-FUNCTIONALIZED DICYCLOPENTADIENE MONOMER AND POLYMER EMBODIMENTS, AND METHODS OF MAKING AND USING SAME

Disclosed herein are embodiments of a bi-functionalized dicyclopentadiene monomer and polymer embodiments formed therefrom. The monomer embodiments exhibit tunability and can be used to form thermally stable homopolymers, copolymers, and/or crosslinked polymers.