1084890-31-2

Basic information

• Product Name: N-(2-azidoethyl)-N-ethylaniline
• Synonyms: N-(2-azidoethyl)-N-ethylaniline
• CAS NO: 1084890-31-2
• Molecular Weight: 190.248
• Mol File: 1084890-31-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(2-azidoethyl)-N-ethylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-azidoethyl)-N-ethylaniline(1084890-31-2)
• EPA Substance Registry System: N-(2-azidoethyl)-N-ethylaniline(1084890-31-2)

Safety Data

• Hazardous Substances Data: 1084890-31-2(Hazardous Substances Data)

Upstream product

• 92-49-9 N-ethyl-N-(2-chloroethyl)aniline 
• 92-50-2 2-( N-ethylanilino)ethanol 
• 1084890-30-1 C₁₁H₁₇NO₃S 

Downstream Products

• 342395-45-3 N-ethyl-N-(2-azidoethyl)-4-(4-nitrophenylazo)aniline 
• 1084890-32-3 N-ethyl-N-(2-azidoethyl)-4-(5-nitro-2-thiazole-azo)aniline 
• 1260401-23-7 (E)-2-(3-(4-((2-azidoethyl)(ethyl)amino)styryl)-5,5-dimethylcyclohex-2-enylidene)malononitrile 
• 1260401-34-0 4-((2-azidoethyl)(ethyl)amino)benzaldehyde 
• 1391754-39-4 C₁₄H₁₃ClN₄O₂ 
• 1299466-57-1 C₁₄H₁₄N₄O₃ 

Relevant articles and documents

FLUORESCENT PROBE FOR ALDH3A1 DETECTION

[Problem to be Solved] To provide a fluorescent probe for ALDH3A1 detection that can be used in flow cytometry adaptable to live cells. [Means of Resolution] A compound represented by general formula (I) or a salt thereof, wherein the compound or salt the

Water-soluble, deep-red fluorescent squaraine rotaxanes

Eight fluorescent squaraine rotaxanes with deep-red absorption/emission wavelengths were prepared and assessed for chemical stability and suitability as water-soluble, fluorescent tracers. The most stable squaraine rotaxanes have four large stopper groups attached to the ends of the encapsulated squaraine, and two members of this structural class have promise as highly fluorescent tracers with rapid renal clearance and very low tissue uptake in living mice.

NOVEL CHROMOPHORIC SILYL PROTECTING GROUPS AND THEIR USE IN THE CHEMICAL SYNTHESIS OF OLIGONUCLEOTIDES

The present invention provides compounds of the formula (I): C-Q-O-Si (R1)(R2)-N wherein C is a chromophore; Q is selected from the group consisting of optionally substituted aliphatic, aryl, heteroaryl, cycloalkyl or heterocycloalkyl; R1 and R2 are independently selected from the group consisting of optionally substituted C1-8 alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C1-8 alkyloxy, cycloalkyloxy, heterocycloalkyloxy, alkylsilyloxy and arylsilyloxy; and N is a glycosylamine or abasic moiety.