26059-38-1

Basic information

• Product Name: Benzenamine, 2-(1-pentynyl)-
• CAS NO: 26059-38-1
• Molecular Formula: C11H13N
• Molecular Weight: 159.231
• Mol File: 26059-38-1.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Benzenamine, 2-(1-pentynyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2-(1-pentynyl)-(26059-38-1)
• EPA Substance Registry System: Benzenamine, 2-(1-pentynyl)-(26059-38-1)

Safety Data

• Hazardous Substances Data: 26059-38-1(Hazardous Substances Data)

Upstream product

• 627-19-0 1-Pentyne 
• 615-43-0 2-iodophenylamine 
• 764-33-0 hex-2-ynoic acid 
• 693-02-7 hex-1-yne 
• 609-73-4 o-nitroiodobenzene 
• 19093-51-7 1-pentynyl copper 
• 344412-67-5 1-nitro-2-(pent-1-yn-1-yl)benzene 

Downstream Products

• 13228-41-6 2-propyl-indole 
• 219700-38-6 Methyl (3S)-3-{N-benzyl-N-[(S)-1-phenylethyl]amino}-6-benzyloxyhexanoate 
• 219700-40-0 (2S,3R)-3-{(S)-4-Benzyloxy-1-[benzyl-((S)-1-phenyl-ethyl)-amino]-butyl}-2-hydroxy-2-methyl-succinic acid dimethyl ester 
• 219700-39-7 (2R,3R)-3-{(S)-4-Benzyloxy-1-[benzyl-((S)-1-phenyl-ethyl)-amino]-butyl}-2-hydroxy-2-methyl-succinic acid dimethyl ester 
• 219700-41-1 (3R,4R,5S)-3-Hydroxy-3-methyl-4-methoxycarbonyl-5-(3'-hydroxypropyl)pyrrolidin-2-one 
• 287477-12-7 (E)-3-(but-1-en-1-yl)-2-phenyl-1H-indole 
• 874796-27-7 1-(4-methoxyphenyl)-3-[2-(1-pentynyl)phenyl]urea 

Relevant articles and documents

Asymmetric Synthesis of 3-Methyleneindolines via Rhodium(I)-Catalyzed Alkynylative Cyclization of N-(o-Alkynylaryl)imines

The first asymmetric synthesis of 3-methyleneindolines from alkynyl imines has been developed via a rhodium-catalyzed tandem process: regioselective alkynylation of the internal alkynes and subsequent intramolecular addition to the imines. The reaction pr

A Synthetic Route to Chiral Benzo-Fused N-Heterocycles via Sequential Intramolecular Hydroamination and Asymmetric Hydrogenation of Anilino-Alkynes

An efficient sequential intramolecular hydroamination/asymmetric hydrogenation reaction under catalysis of a single chiral ruthenium complex or a binary system consisting of achiral gold complex and chiral ruthenium complex has been reported. A diverse range of enantioenriched benzo-fused N-heterocycles, including 1,2,3,4-tetrahydroquinoline, indoline, and 2,3,4,5-tetrahydro-1H-benzo[b]azepine derivatives, were obtained from anilino-alkynes in high yields (up to 98%) with moderate to excellent enantioselectivities (up to 98% ee) under mild conditions. This protocol features good functional group tolerance and high atom economy. Furthermore, this catalytic protocol is applicable to gram-scale synthesis of a naturally occurring alkaloid, (-)-Angustureine.

An efficient synthesis of indoles via a CuMgAl-LDH-catalyzed cyclization of 2-alkynylsulfonanilides

A highly efficient method for the synthesis of indoles has been successfully developed via a CuMgAl-LDH-catalyzed intramolecular annulation reaction of 2-alkynylsulfonanilides. This CuMgAl-LDH catalyst features facile preparation, recovery, and reuse at l