50610-29-2

Basic information

• Product Name: 2-[(5-CHLORO-2-NITROPHENYL)AMINO]ETHANOL
• Synonyms: 2-[(5-CHLORO-2-NITROPHENYL)AMINO]ETHANOL
• CAS NO: 50610-29-2
• Molecular Formula: C₈H₉ClN₂O₃
• Molecular Weight: 216.62
• Mol File: 50610-29-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[(5-CHLORO-2-NITROPHENYL)AMINO]ETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(5-CHLORO-2-NITROPHENYL)AMINO]ETHANOL(50610-29-2)
• EPA Substance Registry System: 2-[(5-CHLORO-2-NITROPHENYL)AMINO]ETHANOL(50610-29-2)

Safety Data

• Hazardous Substances Data: 50610-29-2(Hazardous Substances Data)

Upstream product

• 611-06-3 2,4-dichloronitrobenzene 
• 141-43-5 ethanolamine 
• 610-40-2 3,4-dinitro-chlorobenzene 
• 71-36-3 butan-1-ol 
• 342043-37-2 3,5-dichloro-2-nitroacetanilide 

Downstream Products

• 91721-53-8 1-acetoxy-2-(N-acetyl-5-chloro-2-nitro-anilino)-ethane 
• 181870-03-1 2-[5-(1H-imidazol-1-yl)-2-nitroanilino]ethanol 
• 329922-72-7 2-(2-nitro-5-pyrrodidin-1-ylanilino)-1-ethanol 
• 100417-17-2 3-(2-amino-5-chlorophenyl)-2-iminothiazolidine dihydrochloride 
• 100418-41-5 5-chloro-2-nitro-N-(2-thiocyanatoethyl)-aniline 
• 63387-85-9 2-[(2-amino-5-chlorophenyl)-amino]ethanol 
• 78056-11-8 2-<2-<(tert-butoxycarbonyl)amino>ethyl>-6-chloro-1-<2-(p-toluenesulfonyloxy)ethyl>benzimidazole 
• 78056-08-3 2-(2-aminoethyl)-6-chloro-1-(2-hydroxyethyl)benzimidazole dihydrochloride 
• 100418-35-7 5-chloro-N-(2-mesyloxyethyl)-2-nitroaniline 

Relevant articles and documents

Regulating Cofactor Balance In Vivo with a Synthetic Flavin Analogue

A novel strategy to regulate cofactor balance in vivo for whole-cell biotransformation using a synthetic flavin analogue is reported. High efficiency, easy operation, and good applicability were observed for this system. Confocal laser scanning microscopy was employed to verify that the synthetic flavin analogue can directly permeate into Escherichia coli cells without modifying the cell membrane. This work provides a promising intracellular redox regulatory approach to construct more efficient cell factories.

TRIAZOLO- AND PYRAZOLOQUINAZOLINE DERIVATIVES AS PDE10A ENZYME INHIBITOR

The invention relates to compounds of the formula (I) and their use as pharmaceutical ingredients, in particular for the treatment of CNS related diseases.

Specific features of nucleophilic substitution in 1-chloro-3,4- dinitrobenzene

Effects of the solvent, temperature, and nucleophile nature on the selectivity of nucleophilic substitution in 1-chloro-3,4-dinitrobenzene were studied, and optimal conditions were found for the synthesis and isolation of particular products.