52536-39-7

Basic information

• Product Name: 2-PROP-2-YNYLOXY-PHENYLAMINE
• Synonyms: 2-PROP-2-YNYLOXY-PHENYLAMINE;2-(2-propyn-1-yloxy)aniline(SALTDATA: FREE);2-(prop-2-ynyloxy)benzenamine;2-(2-propyn-1-yloxy)aniline
• CAS NO: 52536-39-7
• Molecular Formula: C₉H₉NO
• Molecular Weight: 147.17386
• Mol File: 52536-39-7.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 82 °C(Press: 40 Torr)
• Appearance: /
• Density: 1 +-.0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 4.02±0.10(Predicted)
• CAS DataBase Reference: 2-PROP-2-YNYLOXY-PHENYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PROP-2-YNYLOXY-PHENYLAMINE(52536-39-7)
• EPA Substance Registry System: 2-PROP-2-YNYLOXY-PHENYLAMINE(52536-39-7)

Safety Data

• Hazardous Substances Data: 52536-39-7(Hazardous Substances Data)

Usage

General Description

2-PROP-2-YNYLOXY-PHENYLAMINE, also known as 2-(prop-2-ynyloxy)aniline, is primarily used in organic synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and other chemical compounds. It is also employed in the development of advanced materials and serves as an important building block for the creation of novel organic molecules. With its unique chemical properties, 2-PROP-2-YNYLOXY-PHENYLAMINE plays a crucial role in facilitating the synthesis of diverse organic compounds and contributes to advancements in the fields of medicine, agriculture, and materials science.

Upstream product

• 6165-75-9 propargyl benzenesulfonate 
• 13350-09-9 1-nitro-2-(prop-2-yn-1-yloxy)benzene 
• 88-75-5 2-hydroxynitrobenzene 
• 98-09-9 benzenesulfonyl chloride 
• 614-80-2 2-(acetylamino)phenol 
• 95-55-6 2-amino-phenol 
• 186663-74-1 tert-butyl (2-hydroxyphenyl)carbamate 

Downstream Products

• 52536-40-0 2-(3-phenylprop-2-ynyloxy)aniline 
• 326598-59-8 1,2-bis[(3'-phenyl-2'-ynyloxy)-2'-amino-phenyl]benzene 
• 326598-56-5 2-[3-(4-methylphenyl)prop-2-ynyloxy]aniline 
• 326598-55-4 2-[3-(3-chloro-phenyl)-prop-2-ynyloxy]-phenylamine 
• 326598-58-7 2-[3-(4-methoxyphenyl)prop-2-ynyloxy]aniline 
• 326598-57-6 2-[3-(2,4-dimethoxy-5-pyrimidinyl)prop-2-ynyloxy]aniline 
• 849064-91-1 (Z)-3-benzylidene-4-acetyl-3,4-dihydro-2H-1,4-benzoxazine 
• 849065-02-7 (R)-3-benzyl-4-acetyl-3,4-dihydro-2H-1,4-benzoxazine 
• 849064-80-8 N-[2-(3-phenylprop-2-ynyloxy)phenyl]acetamide 
• 849064-87-5 N-{2-[3-(4-methylphenyl)prop-2-ynyloxy]phenyl}acetamide 
• 849064-96-6 (Z)-4-acetyl-3-[(4-methoxyphenyl)methylidene]-3,4-dihydro-2H-1,4-benzoxazine 
• 849064-97-7 (Z)-4-acetyl-3-[(2-methoxyphenyl)methylidene]-3,4-dihydro-2H-1,4-benzoxazine 
• 849064-98-8 (Z)-4-acetyl-3-[(4-methylphenyl)methylidene]-3,4-dihydro-2H-1,4-benzoxazine 
• 849064-88-6 N-{2-[3-(2-methylphenyl)prop-2-ynyloxy]phenyl}acetamide 

Relevant articles and documents

Ruthenium-Catalyzed Tandem Carbene/Alkyne Metathesis/N-H Insertion: Synthesis of Benzofused Six-Membered Azaheterocycles

The Cp*RuCl-based catalyst enables expedient access to a variety of benzofused six-membered azaheterocycles from unprotected o-alkynylanilines and trimethylsilyldiazomethane through an unprecedent tandem carbene/alkyne metathesis/N-H insertion reaction. The transformation takes place under mild reaction conditions (room temperature, 15 min) and with excellent functional group tolerance. The synthetic utility of the final products and a mechanistic rationale are also discussed.

Gold nanoparticles anchored onto the magnetic poly(ionic-liquid) polymer as robust and recoverable catalyst for reduction of Nitroarenes

Gold nanoparticles supported on poly ionic-liquid magnetic nanoparticles (MNP@PIL@Au) were synthesized by reduction of HAuCl4 with sodium borohydride. The synthesized catalyst was characterized using by AAS, TEM, FT-IR, EDS, TGA and XRD techniques. The performance of the synthesized catalyst was investigated in the reduction of nitroarenes with NaBH4. The reaction was carried out for various nitroarenes in water and mild conditions with high yields. The catalyst selectivity for the reduction of nitro group in the presences of other functional groups such as halides and alkynes was fairly well. The recycling of the catalyst was done 8 times without any significant loss of its catalytic activity.

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.