C07C2601/20

MATERIAL FOR HOLE-TRANSPORT LAYER, MATERIAL FOR HOLE-INJECTION LAYER, ORGANIC COMPOUND, LIGHT-EMITTING DEVICE, LIGHT-EMITTING APPARATUS, ELECTRONIC DEVICE, AND LIGHTING DEVICE

A material for a hole-transport layer includes a monoamine compound. The first aromatic group, the second aromatic group, and the third aromatic group are bonded to the nitrogen atom of the monoamine compound. The first and second aromatic groups each independently include 1 to 3 benzene rings. One or both of the first and second aromatic groups have one or more hydrocarbon groups each having 1 to 12 carbon atoms each forming a bond only by the sp.sup.3 hybrid orbitals. The total number of the carbon atoms in the hydrocarbon group in the first or second aromatic group is 6 or more. The total number of the carbon atoms in all of the hydrocarbon groups in the first and second aromatic groups is 8 or more. The third aromatic group is a substituted or unsubstituted monocyclic condensed ring or a substituted or unsubstituted bicyclic or tricyclic condensed ring.

COMPOSITIONS AND METHODS FOR TREATING CANCER AND INFLAMMATORY DISEASES

The present disclosure is directed to, e.g., 3-substituted, 5-amine-substituted-cyclohex-2-en-1-one compounds, and method of treatment and making associated with the same compounds.

AROMATIC AMIDES HAVING A FUNGICIDAL ACTIVITY, THEIR AGRONOMIC COMPOSITIONS AND RELATIVE PREPARATION METHOD

Aromatic amides are described, having general formula (I):

##STR00001##

suitably substituted and having a high fungicidal activity, together with their use for controlling phytopathogenic fungi of important agricultural crops.

Normal Alpha Olefin Synthesis Using Dehydroformylation or Dehydroxymethylation

The present invention discloses processes for producing normal alpha olefins, such as 1-hexene, 1-octene, 1-decene, and 1-dodecene in a multistep synthesis scheme from another normal alpha olefin. Also disclosed are reactions for converting aldehydes, primary alcohols, and terminal vicinal diols into normal alpha olefins.

Normal alpha olefin synthesis using dehydroformylation or dehydroxymethylation

The present invention discloses processes for producing normal alpha olefins, such as 1-hexene, 1-octene, 1-decene, and 1-dodecene in a multistep synthesis scheme from another normal alpha olefin. Also disclosed are reactions for converting aldehydes, primary alcohols, and terminal vicinal diols into normal alpha olefins.

COVALENTLY-BOUND POLYBROMOCYCLODODECANE FLAME RETARDANTS

A polybrominated flame-retardant compound, a process for forming a flame-retardant material, and an article of manufacture are disclosed. The polybrominated flame-retardant compound includes a cyclododecane moiety, at least two bromo groups, and at least one substituent having a reactive functional group. The process includes forming a polybromocyclododecane (PBCD) compound having at least one reactive functional group and incorporating the PBCD compound into a polymer in a process that includes covalent binding of the PBCD compound. The article of manufacture includes a flame-retardant material that comprises a polymer with a covalently-bound PBCD compound.

Powerful woody powdery odorant

The present invention relates to the use as perfuming ingredient of a compound of formula ##STR00001##
in the form of any one of its stereoisomers or a mixture thereof, and wherein one dotted line represents a carbon-carbon single bond and the other a carbon-carbon double bond; and R represents a hydrogen atom or a C.sub.1-4 alkyl or alkenyl group; as well as to the perfuming composition and the consumer products containing said compound.

Oxime sulfonate derivatives

Oxime sulfonate compounds of the formula (I), wherein R.sub.1 is O(CO)R.sub.4, COOR.sub.5 or CONR.sub.6R.sub.7; n is 1 or 2; R.sub.2 for example is C.sub.1-C.sub.8alkyl, C.sub.3-C.sub.6cycloalkyl or benzyl; R.sub.3 is for example C.sub.1-C.sub.8alkyl, C.sub.3-C.sub.6cycloalkyl, C.sub.1-C.sub.8haloalkyl, C.sub.2-C.sub.8alkenyl, benzyl, phenyl or naphthyl, which optionally are substituted; R.sub.4 is for example C.sub.1-C.sub.8alkyl, C.sub.3-C.sub.6cycloalkyl, C.sub.1-C.sub.8haloalkyl, C.sub.2-C.sub.8alkenyl, benzyl, phenyl or naphthyl, which optionally are substituted; R.sub.5 is for example C.sub.3-C.sub.20alkyl, C.sub.3-C.sub.14cycloalkyl, C.sub.2-C.sub.8alkenyl, C.sub.1-C.sub.12alkyl which is substituted for example by one or more halogen; or R.sub.5 is phenyl or naphthyl, which are unsubstituted; R.sub.6 and R.sub.7 each independently of one another for example are hydrogen, C.sub.1-C.sub.12alkyl, C.sub.1-C.sub.4haloalkyl, phenyl-C.sub.1-C.sub.4alkyl, C.sub.2-C.sub.8alkenyl or C.sub.3-C.sub.6cycloalkyl, phenyl or naphthyl; or R.sub.6 and R.sub.7, together with the N-atom to which they are attached, form a 5- or 6-membered ring; are suitable as thermal radical initiators. ##STR00001##

Organic compound, light-emitting device, light-emitting apparatus, electronic equipment, lighting device, and electronic device

A novel organic compound is provided. A novel organic compound having a carrier-transport property is provided. A novel organic compound having a hole-transport property is provided. An organic compound having a low refractive index is provided. An organic compound having a low refractive index and a carrier-transport property is provided. An organic compound having a low refractive index and a hole-transport property is provided. An organic compound represented by the following general formula (G1) is provided. ##STR00001##

Method for preparing substituted alkyl cycloalkanones

The present invention relates to a method for producing a substituted alkyl cycloalkanone, comprising the alkylation of a cycloalkanone with an alkene derivative in the presence of a metal oxide, where n is 2 to 20, m is 0 to 10, and R is a functional group.