Category: 477776-17-3

New Advances in Chemical Research, May 2021. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction.Formula: C9H7ClN2, In a article, mentioned the application of 477776-17-3, Name is 6-(Chloromethyl)quinoxaline, molecular formula is C9H7ClN2

The present invention relates to a method for preparing quinoxaline-5- and 6-carboxylic acids. The method comprises contacting an aqueous alkaline suspension of a 5- or 6-halomethyl quinoxaline with oxygen in the presence of a transition metal catalyst, to form the respective quinoxaline-5- or 6-carboxylic acid. The method for oxidizing benzylic methyl groups may also be employed to prepare a wide variety of heterocyclic carboxylic acid compounds.

If you are interested in 477776-17-3, you can contact me at any time and look forward to more communication. Formula: C9H7ClN2

Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1060 | ChemSpider

Reference of 477776-17-3, New research progress on 477776-17-3 in 2021. As an important bridge between the micro and macro material world, chemistry is one of the main methods and means for humans to understand and transform the material world.477776-17-3, Name is 6-(Chloromethyl)quinoxaline, molecular formula is C9H7ClN2. In a article，once mentioned of 477776-17-3

The invention concerns the preparation of compounds of formula STR1 and acid addition and quaternary ammoniun salts thereof, wherein the dotted line represents an optional bond, Ar represents a ring system of formula STR2 in which Q is O, S, –CR7 =CR8 –, –N=CR8 — and –N=N–; R4, R5 and R6, and R7 and R8 when present, each represent hydrogen or a substituent selected from lower alkyl, lower alkenyl, lower alkoxy, NO2, NH2, haloloweralkyl, hydroxyloweralkyl, aminoloweralkyl, substituted amino, halogen, loweralkoxycarbonyl, cyano, CONH2 and hydroxy; and additionally either R4 and R5 when adjacent or R6 and R8 when adjacent, together with the carbon atoms to which they are attached also represent a fused five or six membered carbocylic or heterocyclic ring optionally carrying one or more substituents as defined above; R is an optionally substituted aryl or heteroaryl radical or a cycloalkyl radical containing 5 to 7 carbon atoms; R1, R2, R3 and R9 are each hydrogen or a lower alkyl group; n is 0 or 1; X is =O, =S or =NH; Y is –O– or a direct bond and Z is — CO– or –CH2 –, with the proviso that when Ar is unsubstituted phenyl and R9 is hydrogen then Y is –O–. The compounds of formula I exhibit psychotropic activity and are useful as antidepressants.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 477776-17-3

Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1062 | ChemSpider

Reference of 477776-17-3, New research progress on 477776-17-3 in 2021. In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction. 477776-17-3, Name is 6-(Chloromethyl)quinoxaline, molecular formula is C9H7ClN2. In a Patent，once mentioned of 477776-17-3

The invention concerns the preparation of compounds of formula STR1 and acid addition and quaternary ammonium salts thereof, wherein the dotted line represents an optional bond, Ar represents a ring system of formula STR2 in which Q is O, S, –CR7 =CR8 –, –N=CR8 — and –NM=N–; R4, R5 and R6 ; and R7 and R8 when present, each represent hydrogen or a substituent selected from lower alkyl, lower alkenyl, lower alkoxy, NO2, NH2, haloloweralkyl, hydroxyloweralkyl, aminoloweralkyl, substituted amino, halogen, loweralkoxycarbonyl, cyano, CONH2 and hydroxy; and additionally either R4 and R5 when adjacent or R6 and R8 when adjacent, together with the carbon atoms to which they are attached also represent a fused five or six membered carbocylic or heterocyclic ring optionally carrying one or more substituents as defined above; R is an optionally substituted aryl or heteroaryl radical or a cycloalkyl radical containing 5 to 7 carbon atoms; R1, R2, R3 and R9 are each hydrogen or a lower alkyl group; n is 0 or 1; X is =O, =S, or =NY; Y is –O– or a direct bond and Z is — CO– or –CH2 –, with the proviso that when Ar is unsubstituted phenyl and R9 is hydrogen then v is –O–. The compounds of formula I exhibit psychotropic activity and are useful as antidepressants.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 477776-17-3

Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1063 | ChemSpider

Synthetic Route of 477776-17-3, New research progress on 477776-17-3 in 2021. In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction. 477776-17-3, Name is 6-(Chloromethyl)quinoxaline, molecular formula is C9H7ClN2. In a Patent，once mentioned of 477776-17-3

The present invention relates to a method for preparing quinoxaline-5- and 6-carboxylic acids. The method comprises contacting an aqueous suspension of a 5- or 6-hydroxymethyl quinoxaline with oxygen in the presence of a transition metal catalyst, to form the respective quinoxaline-5- or 6-carboxylic acid. The method for oxidizing benzylic methyl groups may also be employed to prepare a wide variety of heterocyclic carboxylic acid compounds.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 477776-17-3. In my other articles, you can also check out more blogs about 477776-17-3

Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1061 | ChemSpider

Application of 477776-17-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.477776-17-3, Name is 6-(Chloromethyl)quinoxaline, molecular formula is C9H7ClN2. In a Patent，once mentioned of 477776-17-3

Pyridyl- and/or pyridoyl-(piperid-4-yl) ureas and analogues thereof

The invention concerns the preparation of compounds of formula STR1 and acid addition and quaternary ammonium salts thereof, wherein the dotted line represents an optional bond, Ar represents a ring system of formula STR2 in which Q is O, S, –CR7 =CR8 –, –N=CR8 — and –NM=N–; R4, R5 and R6 ; and R7 and R8 when present, each represent hydrogen or a substituent selected from lower alkyl, lower alkenyl, lower alkoxy, NO2, NH2, haloloweralkyl, hydroxyloweralkyl, aminoloweralkyl, substituted amino, halogen, loweralkoxycarbonyl, cyano, CONH2 and hydroxy; and additionally either R4 and R5 when adjacent or R6 and R8 when adjacent, together with the carbon atoms to which they are attached also represent a fused five or six membered carbocylic or heterocyclic ring optionally carrying one or more substituents as defined above; R is an optionally substituted aryl or heteroaryl radical or a cycloalkyl radical containing 5 to 7 carbon atoms; R1, R2, R3 and R9 are each hydrogen or a lower alkyl group; n is 0 or 1; X is =O, =S, or =NY; Y is –O– or a direct bond and Z is — CO– or –CH2 –, with the proviso that when Ar is unsubstituted phenyl and R9 is hydrogen then v is –O–. The compounds of formula I exhibit psychotropic activity and are useful as antidepressants.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 477776-17-3

Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1063 | ChemSpider

Chemistry is traditionally divided into organic and inorganic chemistry. Product Details of 477776-17-3, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 477776-17-3

Method for preparing heterocyclic-carboxylic acids

The present invention relates to a method for preparing quinoxaline-5- and 6-carboxylic acids. The method comprises contacting an aqueous alkaline suspension of a 5- or 6-halomethyl quinoxaline with oxygen in the presence of a transition metal catalyst, to form the respective quinoxaline-5- or 6-carboxylic acid. The method for oxidizing benzylic methyl groups may also be employed to prepare a wide variety of heterocyclic carboxylic acid compounds.

If you are interested in 477776-17-3, you can contact me at any time and look forward to more communication. Product Details of 477776-17-3

Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1060 | ChemSpider

Synthetic Route of 477776-17-3, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Patent, and a compound is mentioned, 477776-17-3, 6-(Chloromethyl)quinoxaline, introducing its new discovery.

Method for preparing heterocyclic-carboxylic acids

The present invention relates to a method for preparing quinoxaline-5- and 6-carboxylic acids. The method comprises contacting an aqueous suspension of a 5- or 6-hydroxymethyl quinoxaline with oxygen in the presence of a transition metal catalyst, to form the respective quinoxaline-5- or 6-carboxylic acid. The method for oxidizing benzylic methyl groups may also be employed to prepare a wide variety of heterocyclic carboxylic acid compounds.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 477776-17-3. In my other articles, you can also check out more blogs about 477776-17-3

Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1061 | ChemSpider

Synthetic Route of 477776-17-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.477776-17-3, Name is 6-(Chloromethyl)quinoxaline, molecular formula is C9H7ClN2. In a Patent£¬once mentioned of 477776-17-3

Piperid-4-yl ureas and thio ureas used as antidepressant agents

The invention concerns the preparation of compounds of formula STR1 and acid addition and quaternary ammoniun salts thereof, wherein the dotted line represents an optional bond, Ar represents a ring system of formula STR2 in which Q is O, S, –CR7 =CR8 –, –N=CR8 — and –N=N–; R4, R5 and R6, and R7 and R8 when present, each represent hydrogen or a substituent selected from lower alkyl, lower alkenyl, lower alkoxy, NO2, NH2, haloloweralkyl, hydroxyloweralkyl, aminoloweralkyl, substituted amino, halogen, loweralkoxycarbonyl, cyano, CONH2 and hydroxy; and additionally either R4 and R5 when adjacent or R6 and R8 when adjacent, together with the carbon atoms to which they are attached also represent a fused five or six membered carbocylic or heterocyclic ring optionally carrying one or more substituents as defined above; R is an optionally substituted aryl or heteroaryl radical or a cycloalkyl radical containing 5 to 7 carbon atoms; R1, R2, R3 and R9 are each hydrogen or a lower alkyl group; n is 0 or 1; X is =O, =S or =NH; Y is –O– or a direct bond and Z is — CO– or –CH2 –, with the proviso that when Ar is unsubstituted phenyl and R9 is hydrogen then Y is –O–. The compounds of formula I exhibit psychotropic activity and are useful as antidepressants.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 477776-17-3

Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1062 | ChemSpider