16398-07-5

Basic information

• Product Name: 2-chloro-N-(2-hydroxyphenyl)-5-nitrobenzamide
• Synonyms: benzamide, 2-chloro-N-(2-hydroxyphenyl)-5-nitro-
• CAS NO: 16398-07-5
• Molecular Formula: C₁₃H₉ClN₂O₄
• Molecular Weight: 292.6746
• Mol File: 16398-07-5.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 390.3°C at 760 mmHg
• Flash Point: 189.9°C
• Density: 1.536g/cm³
• Vapor Pressure: 1.19E-06mmHg at 25°C
• Refractive Index: 1.706
• CAS DataBase Reference: 2-chloro-N-(2-hydroxyphenyl)-5-nitrobenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-N-(2-hydroxyphenyl)-5-nitrobenzamide(16398-07-5)
• EPA Substance Registry System: 2-chloro-N-(2-hydroxyphenyl)-5-nitrobenzamide(16398-07-5)

Safety Data

• Hazardous Substances Data: 16398-07-5(Hazardous Substances Data)

Upstream product

• 25784-91-2 2-chloro-5-nitrobenzoylchloride 
• 95-55-6 2-amino-phenol 
• 2516-96-3 2-chloro-5-nitrobenzoic acid 

Downstream Products

• 23474-66-0 2-amino-10H-dibenzo[b,f][1,4]oxazepin-11-one 
• 1060674-95-4 2-(tert-butylthio)-N-(2-hydroxyphenyl)-5-nitrobenzamide 
• 23474-61-5 2-amino-10-ethyl-10H-dibenzo[b,f][1,4]oxazepin-11-one 
• 140412-87-9 10-Ethyl-2-nitro-10H-dibenzo[b,f][1,4]oxazepin-11-one 
• 54584-72-4 2-(2-chloro-5-nitrophenyl)benzo[d]oxazole 

Relevant articles and documents

Identification of a novel non-carbohydrate molecule that binds to the ribosomal A-site RNA

We report the identification of a novel compound that binds to the Escherichia coli ribosomal A-site. We observed binding using NMR, mass spectrometry, and docking techniques and demonstrate that the compound binds in the same position as occupied by amin

Covalent Occlusion of the RORγt Ligand Binding Pocket Allows Unambiguous Targeting of an Allosteric Site

The nuclear receptor RORγt is a key positive regulator in the differentiation and proliferation of T helper 17 (Th17) cells and the production of proinflammatory cytokines like IL-17a. Dysregulation of this pathway can result in the development of various

Thioimides: New reagents for effective synthesis of thiolesters from carboxylic acids

(Chemical Equation Presented) Thioimides and carboxylic acids are used as the precursors for the convenient synthesis of thiolesters in the phosphine mediated process. Cyclic and acyclic thioimides show equal efficiency, furnishing the desired thiolesters in good to excellent yields. The general, highly efficient transformation tolerates various functional groups and the resulting thiolesters are obtained in high purity after a simple separation. The reaction scope has been demonstrated on the preparation of several highly functionalized target molecules.