35826-31-4

Usage

Uses

Used in Analytical Chemistry:
3-Amino-4-phenylaminopyridine is utilized as a reagent for the detection and quantification of hydrogen peroxide, a critical component in various chemical and biological processes. Its role in this application is pivotal for accurate measurements and analysis.
Used in Medical Diagnostics:
In the medical field, 3-Amino-4-phenylaminopyridine serves as a reagent in the determination of blood sugar levels, which is essential for monitoring and managing diabetes and other related conditions.
Used in Pharmaceutical Synthesis:
3-Amino-4-phenylaminopyridine is also employed in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Research and Development:
3-Amino-4-phenylaminopyridine has shown potential anticancer and anti-inflammatory properties, making it a subject of interest for further research. Its exploration in these areas could lead to advancements in medical treatments.
Used in Organic Chemistry:
In the realm of organic chemistry, 3-Amino-4-phenylaminopyridine is used in the synthesis of other organic compounds, broadening its utility in chemical reactions and product development.
However, due to its potential health hazards and toxic effects, 3-Amino-4-phenylaminopyridine should be handled with caution to ensure safety in all applications.

Upstream product

• 35750-90-4 4-(N-phenylamino)-3-nitropyridine 
• 119-75-5 2-nitro-N-phenylaniline 
• 5470-18-8 2-Chloro-3-nitropyridine 
• 62-53-3 aniline 
• 13091-23-1 4-chloro-3-nitropyridine 

Downstream Products

• 124897-40-1 1-Phenyl-2-pyridin-4-yl-1H-imidazo[4,5-c]pyridine 
• 124897-38-7 1-Phenyl-2-pyridin-2-yl-1H-imidazo[4,5-c]pyridine 
• 61531-50-8 1-Phenyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-thione 
• 61532-35-2 1-phenyl-1H-imidazo[4,5-c]pyridine 
• 98175-84-9 1-phenyl-4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine 
• 129303-82-8 1-phenyl-1H-[1,2,3]triazolo[4,5-c]pyridine 
• 35750-91-5 2-methyl-1-phenylimidazo<4,5-c>pyridine 
• 1078168-12-3 C₁₃H₈F₃N₃ 
• 1033224-92-8 1-phenyl-1,3-dihydro[1,2,5]thiadiazolo[3,4-c]pyridine 2,2-dioxide 

Relevant academic research and scientific papers

Heterocyclic compound and organic light emitting device including the same

Provided are a heterocyclic compound and an organic light-emitting device including the same. The heterocyclic compound may be represented by Formula 1: in the Formula 1, A1, X2, Y1, Y2, m1, m2, R10,R20, R30, b10, b20 and b30 are same as described in the description.

BICYCLIC HETEROCYCLIC DERIVATIVES

Compounds of the formula la or of the formula lb in which X, Y, R1 and R2 have the meanings indicated in Claim 1, are inhibitors of pyruvate dehydrogenase kinase (PDHK), and can be employed, inter alia, for the treatment of diseases

P2X7 MODULATORS

The present invention is directed to compounds of Formulas (I, IIa and IIb): The invention also relates to pharmaceutical compositions comprising compounds of Formulas (I, IIa and IIb). Methods of making and using the compounds of Formulas (I, IIa and IIb) are also within the scope of the invention.

ARYL SULFAMIDE DERIVATIVES AND METHODS OF THEIR USE

The present invention is directed to aryl sulfamide derivatives of formula (I): or a pharmaceutically acceptable salt, stereoisomer or tautomer thereof, which are monoamine reuptake inhibitors, compositions containing these derivatives, and methods of their use for the prevention and treatment of conditions, including, inter alia, vasomotor symptoms, sexual dysfunction, gastrointestinal disorders and genitourinary disorder, depression disorders, endogenous behavioral disorders, cognitive disorders, diabetic neuropathy, pain, and other diseases or disorders.

Structure-guided design of substituted aza-benzimidazoles as potent hypoxia inducible factor-1α prolyl hydroxylase-2 inhibitors

We report the structure-based design and synthesis of a novel series of aza-benzimidazoles as PHD2 inhibitors. These efforts resulted in compound 22, which displayed highly potent inhibition of PHD2 function in vitro.

USE OF TRANSITION METAL CARBENE COMPLEXES IN ORGANIC LIGHT-EMITTING DIODES (OLEDS)

The invention relates to the use of transition metal carbene complexes in organic light-emitting diodes (OLEDS), to a light-emitting layer, a blocking layer for electrons or excitrons or a blocking layer for holes containing these transition metal carbene

(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors

A novel series of imidazo[4,5-c]pyridines bearing a 1,2,5-oxadiazol-3- ylamine functionality has been developed. These are potent inhibitors of mitogen and stress-activated protein kinase-1.

Structure-activity relationships for 1-phenylbenzimidazoles as selective ATP site inhibitors of the platelet-derived growth factor receptor

1-Phenylbenzimidazoles are shown to be a new class of ATP-site inhibitors of the platelet-derived growth factor receptor (PDGFR). Structure- activity relationships (SARs) are narrow, with closely related heterocycles being inactive. A systematic study of

AZABENZIMIDAZOLES IN THE TREATMENT OF ASTHMA, ARTHRITIS AND RELATED DISEASES

A series of imidazo[4,5-c]pyridines which inhibit platelet activating factor (PAF) and also block leukotriene D4 receptors are useful in treating asthma, arthritis, psoriasis, gastrointestinal distress, myocardial infarction, stroke and shock.

Aminopyridine compounds

An aminopyridine compound represented by the formula: STR1 wherein n represents 0 or 1; Z represents =S, =NCN or =CHNO2 ; R1 represents --NR3 R4, --NHNR3 R4, --NHCONHR3 or --NHSO2 R3 ; R2 represents H, or substituted or unsubstituted alkyl; R3 and R4, which may be the same or different, represent H, substituted or unsubstituted alkyl, aryl, substituted or unsubstituted acyl or alkoxycarbonyl group; and R3 and R4 may form a heterocyclic ring together with a nitrogen atom to which R3 and R4 are bound, through another heteroatom or without it; an optical isomer thereof or art acid salt thereof, which is excellent in pharmacological effect and repressed in side effects as a drug for circulatory diseases.