16348-49-5

Basic information

• Product Name: 2-AMINO-N-HYDROXY-BENZAMIDINE
• Synonyms: 2-Aminobenzamidoxime, 97%;Benzenecarboximidamide, 2-amino-N-hydroxy-;2-Amino-N-hydroxybenzimidamide
• CAS NO: 16348-49-5
• Molecular Formula: C₇H₉N₃O
• Molecular Weight: 151.17
• Product Categories: pharmacetical
• Mol File: 16348-49-5.mol
• Article Data: 10

Chemical Properties

• Melting Point: 71-75℃
• Boiling Point: 385.5 °C at 760 mmHg
• Flash Point: 186.9 °C
• Appearance: /
• Density: 1.34 g/cm³
• Vapor Pressure: 1.24E-06mmHg at 25°C
• Refractive Index: 1.631
• Storage Temp.: 2-8°C
• PKA: 6.74±0.69(Predicted)
• CAS DataBase Reference: 2-AMINO-N-HYDROXY-BENZAMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-N-HYDROXY-BENZAMIDINE(16348-49-5)
• EPA Substance Registry System: 2-AMINO-N-HYDROXY-BENZAMIDINE(16348-49-5)

Safety Data

• Hazardous Substances Data: 16348-49-5(Hazardous Substances Data)

Usage

General Description

2-Amino-N-hydroxy-benzamidine is a chemical compound with the molecular formula C7H9N3O2. It is a derivative of benzamidine, which can be used as a potent inhibitor of serine protease enzymes. 2-Amino-N-hydroxy-benzamidine is often used in biochemical research and drug development. It has been studied for its potential applications in treating diseases such as cancer, inflammation, and cardiovascular disorders. The compound is known to have anticoagulant and antithrombotic properties, and its structure makes it a versatile building block for the synthesis of various pharmaceuticals and biologically active compounds.

InChI:InChI=1/C7H9N3O/c8-6-4-2-1-3-5(6)7(9)10-11/h1-4,11H,8H2,(H2,9,10)

Upstream product

• 1885-29-6 anthranilic acid nitrile 
• 612-24-8 o-nitrobenzonitrile 
• 7803-49-8 hydroxylamine 
• 29083-68-9 3-oxy-2-propyl-1,2-dihydro-quinazolin-4-ylamine 
• 108732-43-0 2-Methyl-3-oxy-1,2-dihydro-quinazolin-4-ylamine 

Downstream Products

• 29083-89-4 3-(2-aminophenyl)-5-phenyl-1,2,4-oxadiazole 
• 82216-55-5 2-[5-(4-Nitro-phenyl)-[1,2,4]oxadiazol-3-yl]-phenylamine 
• 94079-14-8 3-(2-Aminophenyl)-5-(4-methoxyphenyl)-1,2,4-oxadiazol 
• 29209-75-4 4-amino-2-(4-nitrophenyl)-1,2-dihydroquinazoline 3-oxide 
• 82216-57-7 2-(5-Benzyl-[1,2,4]oxadiazol-3-yl)-phenylamine 
• 166118-78-1 3-(2-Aminophenyl)-4H-1,2,4-oxadiazol-5-on 
• 29368-93-2 N-[2-(5-phenyl-[1,2,4]oxadiazol-3-yl)-phenyl]-benzamide 
• 29368-92-1 N-[2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-acetamide 
• 82215-93-8 N-(1H-Indazol-3-yl)-4-methyl-benzamide 
• 82215-94-9 4-chloro-N-(1H-indazol-3-yl)benzamide 
• 82216-07-7 N-(1-Benzoyl-1H-indazol-3-yl)-acetamide 
• 82216-33-9 N-[2-(5-Methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-benzamide 
• 82216-59-9 N-[2-(5-Phenyl-[1,2,4]oxadiazol-3-yl)-phenyl]-acetamide 
• 82216-02-2 N-(1-Acetyl-1H-indazol-3-yl)-4-methyl-benzamide 

Relevant articles and documents

A Kinetic Photometric Assay for the Quantification of the Open-Chain Content of Aldoses

Aldoses exist predominantly in the cyclic hemiacetal form, which is in equilibrium with the open-chain aldehyde form. The small aldehyde content hampers reactivity when chemistry addresses the carbonyl moiety. This low concentration of the available aldeh

Construction of Bicyclic 1,2,3-Triazine N-Oxides from Aminocyanides

Using a facile and cost-effective method, nine bicyclic 1,2,3-triazine 2-oxides were synthesized from o-aminocyanide substrates through an unusual nitration cyclization. The reaction mechanism was studied experimentally and theoretically. Moreover, nine 1

Substrate-Independent High-Throughput Assay for the Quantification of Aldehydes

The selective and direct reduction of carboxylic acids into the corresponding aldehydes by chemical methods is still a challenging task in synthesis. Several reductive and oxidative chemical methods are known to produce aldehydes, but most of them require