857349-11-2

Basic information

• Product Name: 4-(4-bromophenyl)-4-pentyn-1-ol
• Synonyms: 4-(4-bromophenyl)-4-pentyn-1-ol
• CAS NO: 857349-11-2
• Molecular Weight: 239.112
• Mol File: 857349-11-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 4-(4-bromophenyl)-4-pentyn-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-bromophenyl)-4-pentyn-1-ol(857349-11-2)
• EPA Substance Registry System: 4-(4-bromophenyl)-4-pentyn-1-ol(857349-11-2)

Safety Data

• Hazardous Substances Data: 857349-11-2(Hazardous Substances Data)

Upstream product

• 5390-04-5 pent-1-yn-5-ol 
• 589-87-7 1,4-bromoiodobenzene 

Downstream Products

• 857349-13-4 6-(4-(5-hydroxy-1-pentynyl)phenyl)-5-hexyn-1-ol 
• 857349-12-3 5-(4-(4-hydroxy-1-butynyl)phenyl)-4-pentyn-1-ol 
• 1366543-67-0 1-bromo-4-(hex-5-en-1-ynyl)benzene 
• 1510847-45-6 C₂₇H₂₄S 
• 1510847-53-6 S-(5-(4-(((9s,10s)-11-(4-(5-(acetylthio)pentyl)phenyl)-12-(anthracen-9-yl)-9,10-dihydro-9,10-ethenoanthracen-9-yl)ethynyl)phenyl)pentyl) ethanethioate 
• 1510847-50-3 S-(5-(4-(anthracen-9-ylethynyl)phenyl)pentyl) ethanethioate 
• 1510847-47-8 S-(5-(4-iodophenyl)pentyl) ethanethioate 
• 1510847-46-7 5-(4-iodophenyl)pentyl methanesulfonate 

Relevant articles and documents

One-Pot Double-Annulation Strategy for the Synthesis of Unusual Fused Bis-Heterocycles

A novel metal-free double-annulation cascade for the construction of unusual fused heterocyclic systems is described. This simple protocol enables the sequential assembly of two rings in one pot from two simple precursors. Acidic conditions promote the condensation and the intramolecular alkynyl Prins reaction of an enyne or arenyne alcohol with a cyclic hemiaminal to form a five-, six-, or seven-membered oxacycle followed by a seven-or eight-membered azacycle. In this transformation, chemical complexity is rapidly generated with the formation of three new bonds (one C-O, one C-C, and one C-N) in one synthetic operation. The strategy is modular and relatively general, providing access to a series of unique fused bicyclic scaffolds.

OXAZOLIDINONE HYDROXAMIC ACID COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS

This invention pertains generally to treating bacterial infections using organic compounds of Formula I. In certain aspects, the invention pertains to treating infections caused by Gram-negative bacteria. (I) wherein X, Y, R1, R2, R3, R4 and R5 and defined herein.

Support curvature and conformational freedom control chemical reactivity of immobilized species

We show that bimolecular reactions between species confined to the surfaces of nanoparticles can be manipulated by the nature of the linker, as well as by the curvature of the underlying particles.