Hexylresorcinol

1,16-Hexadecanedithiol (HDDT) is an alkanethiol that facilitates the formation of self-assembled monolayers (SAMs). It is majorly used to immobilize the surface atoms by attaching the thiol groups.

1-Hexyne reacted with thianthrene cation radical tetrafluoroborate to form trans -1,2- bis (5-thianthreniumyl)alkene tetrafluoroborate . Application 1-Hexyne was used in the synthesis of a tricyclic isoindolinone scaffold by undergoing

1-Hexyne reacted with thianthrene cation radical tetrafluoroborate to form trans -1,2- bis (5-thianthreniumyl)alkene tetrafluoroborate . Application 1-Hexyne was used in the synthesis of a tricyclic isoindolinone scaffold by undergoing

CH₃(CH₂)₃C&equivCH CAS#: 693-02-7 F.W.: 82.15 Stabilized with BHT

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 3-Ethoxysalicylaldehyde was used in the preparation of: Schiff base ligand via condensation with trans -1,2-diaminocyclohexane substituted salen-type Schiff base ligands a new Schiff base,

3-Hexyn-2-ol

3-Hexyn-2-ol

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 3-Hexyne was used in the synthesis of fused hetero-hydropyridyl ligands bonded to the {Ru( p -cymene)} organometallic moiety by reacting with ruthenacycles . It was also used in the preparation of [4+2] cycloaddition product by reacting

Application 3-Hexyne was used in the synthesis of fused hetero-hydropyridyl ligands bonded to the {Ru( p -cymene)} organometallic moiety by reacting with ruthenacycles . It was also used in the preparation of [4+2] cycloaddition product by reacting

CH₃CH₂C&equivCCH₂CH₃ CAS#: 928-49-4 F.W.: 82.15