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Usage

Uses

1. Used in Chemical Synthesis:
1-Aza-1-propyne1-oxide is used as a synthetic intermediate for the production of various organic compounds. Its reactivity with other molecules makes it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
2. Used in Polymer Industry:
In the polymer industry, 1-Aza-1-propyne1-oxide is used as a monomer for the production of specialty polymers with unique properties, such as improved thermal stability, chemical resistance, and mechanical strength. These polymers can be utilized in various applications, including automotive, aerospace, and electronics.
3. Used in Pharmaceutical Industry:
1-Aza-1-propyne1-oxide is used as a key intermediate in the synthesis of certain pharmaceutical compounds, particularly those with potential therapeutic applications. Its ability to form a wide range of chemical bonds allows for the development of new drugs with improved efficacy and reduced side effects.
4. Used in Material Science:
In material science, 1-Aza-1-propyne1-oxide is used in the development of advanced materials with specific properties, such as high-energy-density materials for propulsion systems or materials with tailored electronic properties for use in sensors and electronic devices.
5. Used in Analytical Chemistry:
1-Aza-1-propyne1-oxide can be employed as a reagent in analytical chemistry for the detection and quantification of various compounds. Its unique chemical properties enable selective reactions with target molecules, allowing for accurate and sensitive analysis.

InChI:InChI=1/C23H28N4O4S2/c1-3-26-20(25-10-6-4-5-7-11-25)16(15(2)17(14-24)21(26)30)13-18-22(31)27(23(32)33-18)12-8-9-19(28)29/h13H,3-12H2,1-2H3,(H,28,29)

Upstream product

• 56-41-7 L-alanin 
• 41085-71-6 bromamine T 
• 25854-39-1 sodium nitroethane 
• 98-59-9 p-toluenesulfonyl chloride 
• 75-05-8 acetonitrile 

Downstream Products

• 17492-61-4 1-(3-methyl-4,5-dihydro-isoxazol-5-yl)-ethanone 
• 54605-99-1 (4-methoxyphenyl)(3-methyl-4,5-dihydroioxazol-5-yl)methanone 
• 28164-29-6 2-Hydroxyimino-4-phenyl-but-3-in 
• 5661-30-3 Acetanilidoxim 
• 683-58-9 acetohydroximoyl chloride 
• 74115-67-6 3-Methyl-5-phenyl-3a,6a-dihydro-pyrrolo[3,4-d]isoxazole-4,6-dione 
• 86581-57-9 3,7-Dimethyl-5-phenyl-5,7a-dihydro-[1,2,3]diazaphospholo[3,4-d][1,2,4]oxaphosphole 
• 7064-06-4 3-methyl-5-phenyl-4,5-dihydroisoxazole 
• 89479-66-3 3-Methyl-5-phenyl-isoxazole-4-carbaldehyde 
• 89479-65-2 4-formyl-4,5-dihydro-3-methyl-5-phenylisoxazole 
• 89479-67-4 4,5-dihydro-3-methyl-4-(3-methyl-1,4,2-dioxazol-5-yl)-5-phenylisoxazole 
• 107-46-0 Hexamethyldisiloxane 
• 86260-81-3 O-(Trimethylsilyl)acetohydroximoyl Chloride 
• 25388-20-9 3-methyl-4-phenylisoxazole 

Relevant academic research and scientific papers

Photochemistry of Acetohydroxamic Acid in Solid Argon. FTIR and Theoretical Studies

The products formed during exposure of the CH3CONHOH/Ar (AHA/Ar) matrices to the full output of the Xe lamp and to 225 nm OPO radiation are studied. The irradiation promotes the isomerization, 1Z → 1E, and AHA photodissociation reactions. Four

Photochemical generation of acetonitrile oxide via the C-N bond cleavage of 3-methyl-2-(4-nitrophenyl)-2H-azirine

Acetonitrile oxide (2) is produced by the irradiation of the title azirine 1 in the presence of O2 in fluid solutions and in low-temperature matrices through the capture of the biradical 7 with O2, which is generated by the photochem

Matrix Reactions of Oxygen Atoms with CH3CN. Infrared Spectra of HOCH2CN and CH3CNO

Reactions of oxygen atoms and acetonitrile have been investigated in solid argon at 14-17 K.Primary photoproducts include hydroxyacetonitrile (HOCH2CN) and acetonitrile N-oxide (CH3CNO).Hydroxyacetonitrile forms hydrogen-bonded complexes with acetonitrile and acetonitrile N-oxide as the secondary products.Acetonitrile N-oxide is suggested to be formed by a simple bimolecular addition reaction of atomic oxygen with the nitrile nitrogen.The participation of O(1D) atoms is considered to increase the yield of hydroxyacetonitrile as compared to acetonitrile N-oxide via H-atom abstraction or insertion reactions.The spectral characteristics of hydroxyacetonitrile, acetonitrile N-oxide, and hydrogen-bonded hydroxyacetonitrile-acetonitrile complex isolated in argon matrices are given.

Pathways in the Reactions of Nitronate Ions with Sulphonyl Halides

Primary and tertiary nitronate ions and sulphonyl bromides and iodides rapidly equilibrate with the nitrohalides and sulphinate ion.Products are determined by solvent and by the occurence of cross-equilibrum reactions, some of which have single-electron-transfer mechanism.The reaction of arene-sulphinate and thiolate ions with 1,2-dibromo-2-nitro-1-phenylethane gave E-β-nitrostyrene by Z-philic elimination in both cases, but the more basic thiolate ion also gave, by protophilic elimination, 2-bromo-2-nitro-1-phenylethene.

Kinetics and Mechanism of Oxidation of α-Amino Acids by Bromamine-T in Sulphuric Acid Medium

Kinetics of oxidation of glycine, serine, alanine and leucine by bromamine-T (BAT) have been studied in sulphuric acid (0.05 to 0.15 mol dm-3) at 35 deg C.The reaction shows a first order dependence each in 0, 0 and inverse first order in .Added sulphate ions increase the rate while bisulphate ions retard the reaction.The rate of oxidation increases in the order: leucine > alanine > serine > glycine.The mechanism assumes the interaction of zwitterion of substrate with monobromamine-T in the rate-limiting step.