691-57-6

Usage

Uses

Used in Organic Synthesis:
2-Azidopropane is used as a reagent for introducing azide functional groups into organic compounds, which is crucial for the synthesis of various complex organic molecules and the development of new chemical entities.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-Azidopropane is utilized as a key intermediate in the synthesis of drugs, contributing to the creation of novel therapeutic agents with unique pharmacological properties.
Used in Agrochemical Production:
2-Azidopropane is employed in the development of agrochemicals, where it aids in the synthesis of compounds that are used to protect crops from pests and diseases, thereby enhancing agricultural productivity.
Used in Specialty Chemicals:
2-Azidopropane is also used in the production of specialty chemicals, which are high-value products designed for specific applications in various industries, such as coatings, adhesives, and advanced materials.
Safety Considerations:
Given its explosive nature, 2-Azidopropane requires careful handling and must be managed under stringent safety protocols. This includes proper storage conditions to prevent accidental reactions and adherence to disposal procedures that mitigate risks associated with its hazardous properties.

InChI:InChI=1/C3H7N3/c1-3(2)5-6-4/h3H,1-2H3

Upstream product

• 19935-85-4 methyl n-propylnitrosocarbamate 
• 87549-57-3 (Z)-potassium propanediazotate 

Downstream Products

• 2406-25-9 di-tert-butyl nitroxide 
• 52323-95-2 t-butyl-t-butoxy nitroxide 
• 663885-43-6 4-amino-5-carboxyamido-1-isopropyl-1,2,3-triazole 
• 39786-23-7 1-isopropyl-4-phenyl-1H-1,2,3-triazole 
• 693-13-0 diisopropyl-carbodiimide 
• 304660-28-4 tert-butyl 1-isopropyl-4,5,6,7-tetrahydro-1H-benzo[d][1,2,3]triazole 
• 1613726-68-3 4-((1-iso-propyl-1H-1,2,3-triazol-4-yl)methoxy)benzaldehyde 
• 1429503-73-0 C₂₄H₃₂N₆O₃ 
• 1452772-90-5 1,3-bis(1-isopropyl-1H-1,2,3-triazol-4-yl)-5-(3-methoxy-3-methylbut-1-yn-1-yl)benzene 
• 1268245-61-9 C₁₄H₁₅Cl₂N₃O₂ 
• 40168-14-7 N-(Triphenylphosphoranylidene)isopropylamine 
• 38697-07-3 2-propanimine 
• 74-90-8 hydrogen cyanide 
• 75-05-8 acetonitrile 

Relevant academic research and scientific papers

Reactions of Alkanediazotic Acids at Near Neutral and Basic pH in H2O

The reactions of propane-1-diazotic acid (1) and optically pure (S)-1-phenylethanediazotic acid (2) are investigated in H2O at near neutral (pH 7.0-8.5) and basic (pH > 14) conditions.At near neutral pH, 1 yielded 1- and 2-PrOH (2:1), with both alcohols showing complete incorporation of (18)O from solvent.In the presence of NaN3 the isomeric ratios of azides and alcohols were independent of the ->.The ratio of PrN3 to PrOH is linearly related to ->/ for both primary and secondary products.In basic medium, 1 yields the same isomeric propanol ratio, but both alcohols contain significant and similar amounts of (16)O label. 2 in pH 8.5 buffer gives 1-phenylethanol with 20percent net inversion and containing ca. 4percent (16)O-labeled conservation product.In contrast the ethanolysis of 2 in a basic environment yields 29percent conservation (alcohol) product and the overall stereochemistry of conservation and exchange (ether) products is 1percent net inversion.These results indicate that the extent of (16)O conservation is not dependent on structure, but rather on the degree of proton-transfer-mediated equilibration of the original (16)OH counteranion with H2O, prior to C-N bond cleavage.It is also apparent that a nitrogen-separated ion pair, formed in a two-step process, is responsible for the high yield of rearrangement product, while the stereochemical outcome is determined at the ion-pair stage after nitrogen extrusion.