117507-63-8

Basic information

• Product Name: 2-AMINO-N-FURAN-2-YLMETHYL-BENZAMIDE
• Synonyms: 2-AMINO-N-(2-FURYLMETHYL)BENZAMIDE;2-AMINO-N-FURAN-2-YLMETHYL-BENZAMIDE;AKOS BBB/064
• CAS NO: 117507-63-8
• Molecular Formula: C₁₂H₁₂N₂O₂
• Molecular Weight: 216.24
• Mol File: 117507-63-8.mol
• Article Data: 27

Chemical Properties

• Boiling Point: 444 °C at 760 mmHg
• Flash Point: 222.3 °C
• Appearance: /
• Density: 1.231 g/cm³
• Vapor Pressure: 4.45E-08mmHg at 25°C
• Refractive Index: 1.61
• CAS DataBase Reference: 2-AMINO-N-FURAN-2-YLMETHYL-BENZAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-N-FURAN-2-YLMETHYL-BENZAMIDE(117507-63-8)
• EPA Substance Registry System: 2-AMINO-N-FURAN-2-YLMETHYL-BENZAMIDE(117507-63-8)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 117507-63-8(Hazardous Substances Data)

Usage

General Description

2-Amino-N-furan-2-ylmethyl-benzamide is a chemical compound with the molecular formula C12H12N2O2. It is a white to off-white crystalline powder that is insoluble in water and has a relatively low melting point of 202-204°C. 2-AMINO-N-FURAN-2-YLMETHYL-BENZAMIDE has potential pharmaceutical applications and is used as an intermediate in the synthesis of various organic compounds. It is also used in research and development as a building block for the production of other compounds. However, its specific uses and properties may vary depending on the application and the specific requirements of the user.

InChI:InChI=1/C12H12N2O2/c13-11-6-2-1-5-10(11)12(15)14-8-9-4-3-7-16-9/h1-7H,8,13H2,(H,14,15)

Upstream product

• 617-89-0 furan-2-ylmethanamine 
• 552-89-6 2-nitro-benzaldehyde 
• 134-20-3 2-carbomethoxyaniline 
• 120275-54-9 N-(furan-2-ylmethyl)-2-nitrobenzamide 
• 118-48-9 isatoic anhydride 
• 118-92-3 anthranilic acid 

Downstream Products

• 404933-13-7 N-(4-(5-(3-(furan-2-ylmethyl)-4-oxo-1,2,3,4-tetrahydroquinazolin-2-yl)-2-methoxybenzyloxy)phenyl)acetamide 
• 1253941-38-6 ethyl 2-[2-(furan-2-ylmethylcarbamoyl)phenylamino]-2-oxoacetate 
• 1338824-21-7 N-(4-(5-(3-(furan-2-ylmethyl)-4-oxo-1,2,3,4-tetrahydroquinazolin-2-yl)-2-methoxybenzyloxy)-3,5-dimethylphenyl)acetamide 
• 1338824-23-9 2-(3-((2,6-dimethylphenylthio)methyl)-4-methoxyphenyl)-3-(furan-2-ylmethyl)-2,3-dihydroquinazolin-4(1H)-one 
• 361187-13-5 2-(3-((2,6-dimethylphenoxy)methyl)-4-methoxyphenyl)-3-(furan-2-ylmethyl)-2,3-dihydroquinazolin-4(1H)-one 
• 693234-87-6 N-(2-((2-((furan-2-ylmethyl)carbamoyl)phenyl)carbamoyl)phenyl)furan-2-carboxamide 
• 309926-35-0 C₂₇H₂₃FN₂O₄ 
• 1446789-92-9 2-(cyclohexylamino)-3-((furan-2-yl)methyl)quinazolin-4(3H)-one 
• 1628908-43-9 8-(furan-2-ylmethyl)-4-methoxy-1-methyl-7b,8-dihydro-9H-benzo[6,7][1,4]oxazepino[4,5-a]quinazolin-9-one 
• 885941-84-4 C₁₉H₁₅N₃O₄ 
• 1486520-89-1 C₁₉H₁₇N₃O₂ 
• 1449478-05-0 2-(4-fluorophenyl)-3-((furan-2-yl)methyl)-2,3-dihydrobenzo[d][1,3,2]diazaborinin-4(1H)-one 
• 1422154-64-0 2-((5,5-dimethyl-3-oxocyclohex-1-en-1-yl)amino)-N-(furan-2-ylmethyl)benzamide 
• 1385790-23-7 2-((1-acetyl-3-hydroxy-2-oxoindolin-3-yl)amino)-N-(furan-2-ylmethyl)benzamide 

Relevant articles and documents

Synthesis, crystal structure, vibrational properties and DFT studies of 4-(furan-2-ylmethyl)-1-(thiomorpholinomethyl)-[1,2,4]triazolo[4,3-a]quinazon-5(4H)-one

In this present research, the title compound 4-(furan-2-ylmethyl)-1-(thiomorpholinomethyl)-[1,2,4]triazolo[4,3-a]quinazolin-5(4H)-one(1) was synthesized, and its single crystal was produced in acetone. The use of 1H NMR, 13C NMR, FT-

Synthesis of 2-aryl quinazolinones: Via iron-catalyzed cross-dehydrogenative coupling (CDC) between N-H and C-H bonds

Herein, we describe the direct synthesis of quinazolinones via cross-dehydrogenative coupling between methyl arenes and anthranilamides. The C-H functionalization of the benzylic sp3 carbon is achieved by di-t-butyl peroxide under air, and the subsequent amination-aerobic oxidation process completes the annulation process. Iron catalyzed the whole reaction process and various kinds of functional groups were tolerated under the reaction conditions, providing 31 examples of 2-aryl quinazolinones using methyl arene derivatives in yields of 57-95percent. The synthetic potential has been demonstrated by the additional synthesis of aryl-containing heterocycles. This journal is

A O-aminobenzoyl amine plant growth regulator (by machine translation)

The invention discloses an anthranilic acid amides, structure such as shown in formula I: In the formula R is: The compounds and salts thereof and has very good plant growth regulating activity, spraying through the leaf area of the root and has remarka