52536-40-0

Basic information

• Product Name: 2-(3-phenylprop-2-ynyloxy)aniline
• Synonyms: 2-(3-phenylprop-2-ynyloxy)aniline
• CAS NO: 52536-40-0
• Molecular Weight: 223.274
• Mol File: 52536-40-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(3-phenylprop-2-ynyloxy)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-phenylprop-2-ynyloxy)aniline(52536-40-0)
• EPA Substance Registry System: 2-(3-phenylprop-2-ynyloxy)aniline(52536-40-0)

Safety Data

• Hazardous Substances Data: 52536-40-0(Hazardous Substances Data)

Upstream product

• 1794-48-5 1-bromo-3-phenylprop-2-yne 
• 88-75-5 2-hydroxynitrobenzene 
• 13350-09-9 1-nitro-2-(prop-2-yn-1-yloxy)benzene 
• 52536-42-2 1-Phenyl-3-(2-nitro-phenoxy)-propin-⁽¹⁾ 
• 591-50-4 iodobenzene 
• 52536-39-7 2-(prop-2-ynyloxy)benzenediazonium tetrafluoroborate 

Downstream Products

• 849065-01-6 (Z)-3-benzylidene-4-benzoyl-3,4-dihydro-2H-1,4-benzoxazine 
• 849065-02-7 (R)-3-benzyl-4-acetyl-3,4-dihydro-2H-1,4-benzoxazine 
• 849064-91-1 (Z)-3-benzylidene-4-acetyl-3,4-dihydro-2H-1,4-benzoxazine 
• 849064-90-0 N-[2-(3-phenylprop-2-ynyloxy)phenyl]benzamide 
• 849064-80-8 N-[2-(3-phenylprop-2-ynyloxy)phenyl]acetamide 
• 326598-60-1 4-methyl-N-[2-(3-phenyl-prop-2-ynyloxy)-phenyl]-benzenesulfonamide 
• 52536-38-6 chloro-[2-(3-phenyl-prop-2-ynyloxy)-phenylhydrazono]-acetic acid ethyl ester 
• 52536-44-4 2-ethoxycarbonyl-3-phenyl-4H-pyrazolo[5,1-c][1,4]benzoxazine 

Relevant articles and documents

AgNO3Catalyzed Regio-Selective Synthesis of 3-Alkyl/Aryl-idene-3,4-dihydro-4-tosyl-2H-1,4-Benzoxazine: Novel Anti-Tubercular Scaffolds

A facile and efficient method for the construction of 3-alkyl/aryl substituted 1,4-benzoxazine and benzoxazepine via AgNO3catalyzed cyclization of propargyloxy sulfonamides and their anti-tubercular activity against Mycobacterium tuberculosis H37RVis described. This cyclization proceeds through 6-exo-dig manner to generate the products in moderate to good yields.

Synthesis and highly enantioselective hydrogenation of exocyclic enamides: (Z)-3-arylidene-4-acetyl-3,4-dihydro-2H-1,4-benzoxazines

(Chemical Equation Presented) Highly enantioselective hydrogenation of exocyclic enamides, (Z)-3-arylidene-4-acyl-3,4-dihydro-2H-benzoxazines, was achieved in up to 98.6% ee by using Rh/(R,R)-Me-Duphos complex as the catalytic system. The absolute configu