29483-74-7

Basic information

• Product Name: Benzenamine, 2-(2-benzoxazolyl)-
• CAS NO: 29483-74-7
• Molecular Formula: C13H10N2O
• Molecular Weight: 210.235
• Mol File: 29483-74-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzenamine, 2-(2-benzoxazolyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2-(2-benzoxazolyl)-(29483-74-7)
• EPA Substance Registry System: Benzenamine, 2-(2-benzoxazolyl)-(29483-74-7)

Safety Data

• Hazardous Substances Data: 29483-74-7(Hazardous Substances Data)

Upstream product

• 95-55-6 2-amino-phenol 
• 88-17-5 2-(trifluoromethyl)benzenamine 
• 51674-05-6 1-(2-Aminophenyl)-1-phenyl-methanonoxim 
• 118-48-9 isatoic anhydride 
• 90-04-0 2-methoxy-phenylamine 
• 5348-24-3 2-hydroxy-N-(2-nitrobenzylidene)-aniline 
• 552-89-6 2-nitro-benzaldehyde 
• 840-37-9 2-(2′-nitrophenyl)-1,3-benzoxazole 
• 529-23-7 o-aminobenzaldehyde 
• 5344-90-1 2-Aminobenzyl alcohol 

Downstream Products

• 1092936-36-1 2-[2-(t-Boc-L-alanylamino)phenyl]benzoxazole 
• 1310352-09-0 2-[2-(t-Boc-β-alanylamino)phenyl]benzoxazole 
• 1085705-88-9 2-[(2-L-alanylamino)phenyl]benzoxazole 
• 1297365-28-6 C₁₅H₁₁ClN₂O₂ 
• 378230-76-3 2-(2-(n-octanesulfonylamino)phenyl)benzoxazole 
• 42143-49-7 N-(2-(benzo[d]oxazol-2-yl)phenyl)-4-methylbenzenesulfonamide 

Relevant articles and documents

BiCl3 – An eco-friendly catalyst for an efficient synthesis of benzoxazoles at room temperature

A simple and efficient protocol has been developed for the synthesis of 2-arylbenzoxazole derivatives of potential pharmaceutical interest. The method involves reaction between 2-aminophenol and substituted aromatic aldehydes in the presence of anhydrous bismuth trichloride as catalyst in acetonitrile. The use of eco-friendly bismuth trichloride, overall mild reaction conditions, and moderate to good yield of products are some attractive features of this methodology.

2-Arylbenzothiazole, benzoxazole and benzimidazole derivatives as fluorogenic substrates for the detection of nitroreductase and aminopeptidase activity in clinically important bacteria

A series of 2-(2-nitrophenyl)benzothiazole 7, 2-(2-nitrophenyl)benzoxazole 10 and 2-(2-nitrophenyl)benzimidazole 13 derivatives have been synthesised and assessed as indicators of nitroreductase activity across a range of clinically important Gram negativ

On the purity of 2-[ortho-anilinyl]-1,3-benzoxazole derived from 2H-3,1-benzoxazine-2,4(1H)dione (isatoic anhydride) [1,2]

(Chemical Equation Presented) The Lewis acid catalyzed synthesis and chromatographic purification of isatoic anhydride-derived 2-(2′-anilinyl)- 1,3-benzoxazole (2) can result in the co-isolation of 2 and a light pink colored impurity (a predictable intermediate in the formation of 2. Compound 3 crystallizes in an orthorhombic crystal system of space group P2 12121 with four molecules in the unit cell (α = β = γ = 90°; a = 6.715 (2) A, b = 12.100 (4) A, c = 13.321 (4) A; V = 1082.2 (6) A3). Pure 2 is characterized as a colorless, high-melting solid; unlike the dark colored oil that is isolated if 2 contains traces of 3.