871-31-8

Usage

Uses

Used in Pharmaceutical Industry:
1-Azidoethane is used as a reagent for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agricultural Chemicals Industry:
1-Azidoethane is used as a reagent in the production of agricultural chemicals, aiding in the creation of effective and innovative products for crop protection and enhancement.
Used in Advanced Materials Industry:
1-Azidoethane is used as a reagent for the synthesis of advanced materials, playing a role in the development of cutting-edge technologies and applications.

InChI:InChI=1/C2H5N3/c1-2-4-5-3/h2H2,1H3

Upstream product

• 74-85-1 ethene 
• 98071-92-2 1-ethoxy-1,1-diazido-ethane 
• 122-39-4 diphenylamine 

Downstream Products

• 103095-68-7 1-ethyl-4-phenyl-1H-1,2,3-triazole 
• 47182-04-7 ethyl-triphenylphosphoranyliden-amine 
• 63980-20-1 1,3-Diethyltriazene 
• 74-90-8 hydrogen cyanide 
• 74-86-2 acetylene 
• 102942-92-7 3-ethyl-5-phenyl-3H-[1,2,3]triazol-4-ylamine 
• 63540-08-9 Cyclohexyl-ethyl-carbodiimide 
• 61013-61-4 ethyl 2-azido-3-phenylacrylate 
• 1191128-21-8 1-ethyl-4-(p-tolyl)-1H-1,2,3-triazole 
• 1443767-11-0 C₆₆H₉₆N₃₀O₁₂ 
• 1260217-92-2 C₂₁H₁₉BrClN₂O₂P 
• 1260217-86-4 C₂₁H₁₉Cl₂N₂O₂P 

Relevant academic research and scientific papers

NEW SYNTHETIC "TRICKS". FROM ALIPHATIC AMINES AND AMIDES TO AZIDES AND/OR HOW TO CONVERT RNHCOR' INTO RNHCOR" AVOIDING DRASTIC HYDROLYSES

Controlled reduction of N-alkyl-N-nitrosoamides to hydrazides followed by nitrosation and fragmentation affords azides in 80percent overall yields, under mild conditions.This simple idea is the basis of methods for the conversion of alkylamines and N-alkylamides to alkyl azides, of RNHCOR' into RNHCOR" or RN(COR''')2, and of lactames into ω-azido esters or ω-azido acids.

Reactions of NH Radicals. III. Photolysis of HN3 in the Presence of C2H4 at 313 nm

Photolysis of HN3 vapor in the presence of C2H4 was studied at 313 nm and 30 deg C.The main products were N2, H2, CH4, C2H6, NH4N3, C2H5N * HN3 (salt of C2H5N (azomethines) with HN3), HCN, CH3CN, CH3N3, and C2H5N3.The quantum yields of these products were measured as a function of the light intensity and pressures of HN3 and C2H4.The following mechanism for the main reactions was infered: HN3 + hv(313 nm) -> NH(a1Δ) + N2; NH(a1Δ) + HN3 -> 2N2 + 2H (2a); NH(a1Δ) + HN3 -> NH2 + N3 (2b); NH(a1Δ) + HN3 -> N2 + N2H2* (2c); NH(a1Δ) + C2H4 -> C2H5N* (aziridine and vinylamine) (3); C2H5N* -> CH3 + CH2N (4); C2H5N* -> H2 + CH3CN (5); C2H5N* -> H + C2H4N (6); C2H5N* -> C2H3 + NH2 (7).The rate constant ratios at 30 deg C are: k3/k2 = 1.64; k5/k4 = 0.102; k6/k4 = 0.564; k7/k4 = 0.734.The collisional deactivation from NH(a1Δ) to NH(X3Σ-) by C2H4 was not found.The lifetime of C2H5N* is much shorter than 6.8 * 10-11 s for C2H5NH2*(1Δ) + C2H6)).The relative and absolute rates for the reactions of NH(a1Δ) with HN3, Xe, C2H6, and C2H4 are discussed.