175135-19-0

Usage

Uses

Used in Cosmetics Industry:
5-Morpholino-2-nitrophenol is used as a UV absorber in sunscreen formulations for its ability to protect the skin from harmful ultraviolet radiation. Its inclusion in sunscreens helps to prevent sunburn and reduce the risk of skin cancer, while also minimizing the damaging effects of UV rays on the skin.
Used in Dye Production:
In the dye industry, 5-Morpholino-2-nitrophenol serves as a key intermediate in the synthesis of various dyes. Its chemical structure allows for the creation of dyes with specific color properties, making it valuable for the development of new dyes with unique characteristics.
Used in Pharmaceutical Industry:
5-Morpholino-2-nitrophenol is utilized as a building block in the production of pharmaceuticals. Its unique structure and reactivity make it a promising candidate for the development of new drugs with novel therapeutic properties.
Used in Organic Synthesis:
As an intermediate in organic synthesis, 5-Morpholino-2-nitrophenol is employed in the preparation of a wide range of organic compounds. Its versatility in chemical reactions allows for the synthesis of various target molecules, making it a valuable tool in the field of organic chemistry.
Used in Antimicrobial Development:
5-Morpholino-2-nitrophenol has demonstrated potential as an inhibitor of enzymes involved in the biosynthesis of bacterial cell walls. This property makes it a target for the development of new antimicrobial agents, which could help combat antibiotic-resistant bacteria and contribute to the discovery of novel treatments for bacterial infections.

InChI:InChI=1/C10H12N2O4/c13-10-7-8(1-2-9(10)12(14)15)11-3-5-16-6-4-11/h1-2,7,13H,3-6H2/p-1

Upstream product

• 110-91-8 morpholine 
• 446-36-6 5-fluoro-2-nitrophenol 
• 611-07-4 5-chloro-2-nitrophenol 

Downstream Products

• 1024611-37-7 N-(2-methoxy-4-morpholinophenyl)-6-(thiazol-2-yl)quinazolin-4-amine 
• 209960-91-8 2-methoxy-4-morpholinoaniline 
• 25912-15-6 2-amino-5-morpholinophenol 
• 6950-88-5 4-(3-methoxy-4-nitro-phenyl)morpholine 
• 869790-50-1 4-(4-morpholinyl)-2-(2-iodobenzyloxy)aniline 

Relevant academic research and scientific papers

Nucleophilic substitution of halogens with amines in 2- and 4-nitrophenols

Fluorine and chlorine in halonitrophenols are efficiently replaced with alkylamines in acetonitrile or in an excess of the amine at elevated temperature. Georg Thieme Verlag Stuttgart.

HMOX1 inducers

The present invention is related to compounds of structure (I) as heme oxygenase 1 (HMOX 1) inducers. The present invention is also related a method of controlling the activity or the amount, or both the activity and the amount, of heme-oxygenase 1 in a mammalian subject. The definitions of the variables are provided herein.

ANTIBIOTIC COMPOUNDS

The present invention relates to antibiotic compounds of formula (I), to compositions containing these compounds and to methods of treating bacterial diseases and infections using the compounds. The compounds find application in the treatment of infection with, and diseases caused by, Gram-positive and/or Gram-negative bacteria, and in particular in the treatment of infection with, and diseases caused by, Neisseria gonorrhoeae.

N-(2-acetyl-4-morpholinophenyl amide derivatives for inducing differentiation of mesenchymal stem cells to endothelial cells

The present invention refers to mesenchymal stem cells the vascular endothelial cells inducing their differentiation to the rarity piperidinyl/molpholine for containing amide derivatives and provides use thereof in medicaments. Said amide derivatives the middle ply treated with a vascular endothelial mesenchymal stem cells specifically cells differentiation induction, and are by using an balloon expansion alcoholic beverage like damage for vascular endothelial cells, such as by a vascular event for the effective treatment is enabled.

2-Aminobenzoxazole ligands of the hepatitis C virus internal ribosome entry site

2-Aminobenzoxazoles have been synthesized as ligands for the hepatitis C virus (HCV) internal ribosome entry site (IRES) RNA. The compounds were designed to explore the less basic benzoxazole system as a replacement for the core scaffold in previously discovered benzimidazole viral translation inhibitors. Structure-activity relationships in the target binding of substituted benzoxazole ligands were investigated.

1,2-Di(cyclic)substituted benzene compounds

In one aspect, the present invention provides compounds having formula (1) or (100), a salt thereof or a hydrate of the foregoing, which compounds exhibit excellent cell adhesion inhibitory action or cell infiltration inhibitory action, and are useful as therapeutic or prophylactic agents for various inflammatory diseases and autoimmune diseases associated with adhesion and infiltration of leukocytes, such as inflammatory bowel disease (particularly ulcerative colitis or Crohn's disease), irritable bowel syndrome; rheumatoid arthritis, psoriasis, multiple sclerosis, asthma and atopic dermatitis. wherein R10 represents optionally substituted cycloalkyl, etc., R20-23 represent hydrogen, alkyl, alkoxy, etc., R30-32 represent hydrogen, alkyl, oxo, etc., and R40 represents optionally substituted alkyl, etc.