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Company Website4-penten-1-ol forms ester bond at the C terminus of the linear peptide in solution with HATU as coupling agent.
More Information Supplier Page4-Pentenenitrile (4-PN) is a terminal alkene nitrile. It is obtained from 3-pentenenitrile via cationic nickel hydride or cobalt catalyzed isomerization. 4-Pentenenitrile undergoes hydrocyanation in the presence of bidentate nickel complexes (catalysts) to yield 3-pentenenitrile. 4-PN undergoes gas-phase reaction with OH radicals and Cl atoms in the presence of synthetic air and various reference compounds.
More Information Supplier PageThe sulfonation of 4-pentenoic acid (Allylacetic acid) yields the corresponding γ-lactone.
More Information Supplier Page4-Pentenoyl chloride has been identified as a key impurity in 5-chlorovaleroyl chloride (5-CVC). 4-Pentenoyl chloride can be synthesized by reacting thionyl chloride and 4-pentenoic acid.
More Information Supplier PageMechanism of (THF)W(CO)5-promoted endo- and exo-cycloisomerization of 4-pentyn-1-ol was studied.
More Information Supplier Page4-Pentyn-2-ol, a secondary homopropargylic alcohol, is toxic with LC50 value of 160.
More Information Supplier Page4-Pentynoic acid undergoes copper-catalyzed intramolecular cyclizations to form enol lactones. It also reacts with 1-bromo-1-alkynes in the presence of a Pd catalyst to yield biologically active ynenol lactones.
More Information Supplier Page4-Phenoxybenzoic acid was converted to its corresponding amide by the soil bacterium Bacillus cereus Tim-r01.
More Information Supplier Page4-Phenoxybenzonitrile can be prepared from the tris(3,6-dioxaheptyl)amine-catalyzed nucleophilic aromatic substitution reaction of 4-chlorobenzonitrile with phenol. It can also be prepared by reacting 4-cyanophenol, iodobenzene and CsF/Clinoptilolite (CsF/CP) in DMSO.
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