629-05-0 | 1-Octyne

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$20.00	$14.00
5g	97%	in stock	$45.00	$32.00
25g	97%	in stock	$121.00	$85.00
100g	97%	in stock	$386.00	$270.00

Description

• Catalog Number: AB58670
• Chemical Name: 1-Octyne
• CAS Number: 629-05-0
• Molecular Formula: C8H14
• Molecular Weight: 110.19676
• MDL Number: MFCD00009546
• SMILES: CCCCCCC#C

Computed Properties

• Complexity: 73.3
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Rotatable Bond Count: 4
• XLogP3: 3.5

Literature

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• Effects of trehalose polycation end-group functionalization on plasmid DNA uptake and transfection.

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• Synthesis of ferrocene-labeled steroids via copper-catalyzed azide-alkyne cycloaddition. Reactivity difference between 2β-, 6β- and 16β-azido-androstanes.

  Steroids 20120601

• Total synthesis of (±)-cylindricine C.

  Organic letters 20110916

• Gold(I) catalysts with bifunctional P, N ligands.

  Inorganic chemistry 20110815

• Strain-promoted 'click' chemistry for terminal labeling of DNA.

  Bioconjugate chemistry 20110720

• Analysis of the oxidation of short chain alkynes by flavocytochrome P450 BM3.

  Metallomics : integrated biometal science 20110401

• An insight into the radical thiol/yne coupling: the emergence of arylalkyne-tagged sugars for the direct photoinduced glycosylation of cysteine-containing peptides.

  The Journal of organic chemistry 20110121

• Dihydroceramide desaturase inhibition by a cyclopropanated dihydroceramide analog in cultured keratinocytes.

  Journal of lipids 20110101

• Alkyne-stabilized ruthenium nanoparticles: manipulation of intraparticle charge delocalization by nanoparticle charge States.

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• At the frontier between heterogeneous and homogeneous catalysis: hydrogenation of olefins and alkynes with soluble iron nanoparticles.

  Dalton transactions (Cambridge, England : 2003) 20100928

• Chemical sensing using fiber cavity ring-down spectroscopy.

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• Copper-catalyzed sonogashira-type reactions under mild palladium-free conditions.

  Organic letters 20080807

• Carbocyclization reaction of omega-iodo- and 1,omega-diiodo-1-alkynes without the loss of iodine atoms through a carbenoid-chain process.

  The Journal of organic chemistry 20080104

• Evaluation of the enantiomers of 1-octen-3-ol and 1-octyn-3-ol as attractants for mosquitoes associated with a freshwater swamp in Florida, U.S.A.

  Medical and veterinary entomology 20071201

• An inhibitory sex pheromone tastes bitter for Drosophila males.

  PloS one 20070101

• New coupling reaction of secondary amines, aldehydes, and alkynes catalyzed by an iridium complex.

  Organic letters 20060608

• Adducts of thianthrene- and phenoxathiin cation radical tetrafluoroborates to 1-alkynes. Structures and formation of 1-(5-thianthreniumyl)- and 1-(10-phenoxathiiniumyl)alkynes on alumina leading to alpha-ketoylides and alpha-ketols.

  The Journal of organic chemistry 20051125

• Rhodium-catalyzed nondecarbonylative addition reaction of ClCOCOOC2H5 to alkynes.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20050606

• Effects of 2-alkynyladenosine derivatives on intraocular pressure in rabbits.

  European journal of pharmacology 20040223

• Rhodium-catalyzed regio- and stereoselective 1-seleno-2-thiolation of 1-alkynes.

  The Journal of organic chemistry 20031114

• Synthesis and evaluation of a C8 stationary phase on a silica hydride surface by hydrosilation of 1-octyne.

  Journal of chromatography. A 20030411

• A synthesis of the phenolic lipid, 3-[(Z)-pentadec-8-enyl] catechol, (15:1)-urushiol.

  Chemistry and physics of lipids 20021201