6108-74-3

Basic information

• Product Name: N-(3-aminopropyl)benzamide
• Synonyms: N-(3-aminopropyl)benzamide;N-(3-Aminopropyl)benzamide HCl;Benzamide,N-(3-aminopropyl)-
• CAS NO: 6108-74-3
• Molecular Formula: C₁₀H₁₄N₂O
• Molecular Weight: 178.23
• Mol File: 6108-74-3.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 386.2°C at 760 mmHg
• Flash Point: 187.3°C
• Appearance: /
• Density: 1.07g/cm³
• Vapor Pressure: 3.61E-06mmHg at 25°C
• Refractive Index: 1.545
• CAS DataBase Reference: N-(3-aminopropyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-aminopropyl)benzamide(6108-74-3)
• EPA Substance Registry System: N-(3-aminopropyl)benzamide(6108-74-3)

Safety Data

• Hazardous Substances Data: 6108-74-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H14N2O/c11-7-4-8-12-10(13)9-5-2-1-3-6-9/h1-3,5-6H,4,7-8,11H2,(H,12,13)

Upstream product

• 25099-77-8 2-phenyl-1,4,5,6-tetrahydropyrimidine 
• 98902-03-5 N-(3-benzylaminopropyl)benzamide 
• 88192-19-2 3-azidopropylamine 
• 98-88-4 benzoyl chloride 
• 109-76-2 Trimethylenediamine 
• 618-39-3 benzamidin 
• 55-21-0 benzamide 
• 10364-94-0 1-benzoylimidazole 
• 10517-44-9 1,3-diaminopropane dihydrochloride 
• 23405-15-4 benzoic acid N-hydroxysuccinimide ester 
• 65-85-0 benzoic acid 

Downstream Products

• 75120-94-4 N-[3-(Toluene-4-sulfonylamino)-propyl]-benzamide 
• 1190955-45-3 C₂₀H₁₈FN₃O₃ 
• 1223080-86-1 C₂₆H₂₃BrFN₅O₂ 
• 1446714-10-8 N-[3-(tritylamino)propyl]benzamide 
• 1446714-16-4 N-(3-{acetyl[(trifluoromethyl)sulfonyl]amino}propyl)benzamide 
• 1446714-09-5 N-(3-{[(trifluoromethyl)sulfonyl]amino}propyl)benzamide 
• 5824-62-4 N-[3-(acetylamino)propyl]benzamide 
• 313350-18-4 N₁-[3-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)propyl]benzamide 
• 313350-07-1 N₁-{3-[(3-nitroquinolin-4-yl)amino]propyl}benzamide 
• 98902-03-5 N-(3-benzylaminopropyl)benzamide 
• 65189-53-9 N-[3-(4-Amino-6,7-dimethoxy-quinazolin-2-ylamino)-propyl]-benzamide; hydrochloride 

Relevant articles and documents

Solid phase chemistry at a modified cathode surface. First synthesis of a polyamine precursor

The synthesis of a polyamine precursor was performed at a modified electrode interface. The chemical behaviour of the polythiophene matrix appeared identical to that of polystyrene beads. The target molecule, obtained with good yield, was released from the solid support by cathodic S-N bond scission, using the conducting properties of the polymer. (C) 2000 Elsevier Science Ltd.

SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION

Disclosed are small molecules against cereblon to enhance effector T cell function. Methodos of making thes molecules and methods of using them to treat various disease states are also disclosed.

Preparation method and applications of aromatic heterocyclic compound adopted as selective JAK3 and/or JAK1 kinase inhibitor

The present invention relates to an aromatic heterocyclic compound, a preparation method and applications thereof, wherein the structure of the compound is represented by a general formula (I), each group is defined in the specification, and the compound