69611-44-5

Basic information

• Product Name: N-(2-Butynyl)benzenamine
• Synonyms: N-(2-Butynyl)benzenamine;N-but-2-ynylaniline
• CAS NO: 69611-44-5
• Molecular Formula: C₁₀H₁₁N
• Molecular Weight: 0
• Mol File: 69611-44-5.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-Butynyl)benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-Butynyl)benzenamine(69611-44-5)
• EPA Substance Registry System: N-(2-Butynyl)benzenamine(69611-44-5)

Safety Data

• Hazardous Substances Data: 69611-44-5(Hazardous Substances Data)

Upstream product

• 3355-28-0 1-Bromo-2-butyne 
• 62-53-3 aniline 
• 61493-85-4 but-2-yn-1-yl methanesulfonate 
• 99359-66-7 N-(3-chloro-but-2-enyl)-aniline 

Downstream Products

• 104829-41-6 N-but-2-ynyl-acetanilide 
• 60011-48-5 N-benzyl-N-(3-methyl-2-butyne)aniline 
• 1007389-72-1 3-benzyl-5-ethylidene-1,3-oxazolidin-2-one 
• 491-35-0 C₆H₄NCH₂CHCCH₂ 
• 22514-60-9 1,2-dihydrolepidine 
• 1287759-55-0 N-(but-2-yn-1-yl)-N-(2-hydroxyphenyl)benzamide 
• 4828-94-8 (+/-)-2-(1'-methylallyl)aniline 
• 25706-25-6 α-(-2-Butinyl)-phenylhydrazin 
• 35755-80-7 (E)-N-(2-butenyl)aniline 
• 62722-94-5 (Z)-N-(but-2-en-1-yl)aniline 

Relevant articles and documents

DIACYLGLYCEROL KINASE MODULATING COMPOUNDS

The present disclosure provides diacylglycerol kinase modulating compounds, and pharmaceutical compositions thereof, for treating cancer, including solid tumors, and viral infections, such as HIV or hepatitis B virus infection. The compounds can be used alone or in combination with other agents.

AgNO2 as the NO Source for the Synthesis of Substituted Pyrazole N-Oxides from N-Propargylamines

A straightforward method for synthesizing the pyrazole N-oxides from N-propargylamines and AgNO2 through oxidation/cyclization reaction had been developed. AgNO2 was used as the NO source for the first time to synthesize pyrazole N-o

Enantioselective hydroformylation of aniline derivatives

We have developed a ligand that reversibly binds to aniline substrates, allowing for the control of regioselectivity and enantioselectivity in hydroformylation. In this paper we address how the electronics of the aniline ring affect both the binding of the substrate to the ligand and the enantioselectivity in this reaction.