556-56-9 | Allyl iodide

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$19.00	$13.00
5g	95%	in stock	$31.00	$22.00
25g	95%	in stock	$81.00	$57.00
100g	95%	in stock	$242.00	$170.00
500g	95%	in stock	$1,022.00	$716.00

Description

• Catalog Number: AB45523
• Chemical Name: Allyl iodide
• CAS Number: 556-56-9
• Molecular Formula: C3H5I
• Molecular Weight: 167.9763
• MDL Number: MFCD00001094
• SMILES: ICC=C
• NSC Number: 18588

Computed Properties

• Complexity: 17.2
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 4
• Rotatable Bond Count: 1
• XLogP3: 2.1

Literature

• Reactions of propargyl compounds containing a cyclobutyl group induced by a ruthenium complex.

  Chemistry, an Asian journal 20121101

• Gas-phase reactivity of group 11 dimethylmetallates with allyl iodide.

  Journal of the American Chemical Society 20120208

• Effects of a hydroxyl substituent on the reactivity of the 2,4,6-tridehydropyridinium cation, an aromatic σ,σ,σ-triradical.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20120116

• Palladium-catalyzed allyl cross-coupling reactions with in situ generated organoindium reagents.

  Chemistry, an Asian journal 20110801

• Structure and reactivity of the cysteine methyl ester radical cation.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20110117

• Oxidation state, aggregation, and heterolytic dissociation of allyl indium reagents.

  Journal of the American Chemical Society 20100505

• Gas-phase reactivity of protonated 2-, 3-, and 4-dehydropyridine radicals toward organic reagents.

  The journal of physical chemistry. A 20091210

• N-Cyclo-hexyl-N-(prop-2-en-1-yl)benzene-sulfonamide.

  Acta crystallographica. Section E, Structure reports online 20091201

• Theoretical study on the halogen-zinc exchange reaction by using organozincate compounds.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090602

• C-C bond coupling between the organometallic cations CH3Ag2+, CH3Cu2+ and CH3AgCu+ and allyliodide.

  Dalton transactions (Cambridge, England : 2003) 20090421

• Gas phase synthesis, structure and unimolecular reactivity of silver iodide cluster cations, Ag(n)I(m)(+) (n = 2-5, 0 < m < n).

  Dalton transactions (Cambridge, England : 2003) 20080614

• Gas-phase synthesis of the homo and hetero organocuprate anions [MeCuMe]-, [EtCuEt]-, and [MeCuR]-.

  Journal of the American Chemical Society 20080123

• Cis double allylation of cyclopropenes using cyclopropylindium reagents.

  Organic & biomolecular chemistry 20070707

• Determination of spin-orbit branching fractions in the photodissociation of halogenated hydrocarbons.

  The journal of physical chemistry. A 20070517

• The use of chiral lithium amides in the desymmetrisation of N-trialkylsilyl dimethyl sulfoximines.

  Beilstein journal of organic chemistry 20070101

• Letter: Silver mediated ester bond formation in the gas phase: substrate structure is important.

  European journal of mass spectrometry (Chichester, England) 20070101

• The stability of allyl radicals following the photodissociation of allyl iodide at 193 nm.

  The Journal of chemical physics 20061014

• Ultraviolet photochemistry of trichlorovinylsilane and allyltrichlorosilane: vinyl radical (HCCH2) and allyl radical (H2CCHCH2) production in 193 nm photolysis.

  Physical chemistry chemical physics : PCCP 20060521

• Shock wave study on the thermal unimolecular decomposition of allyl radicals.

  The journal of physical chemistry. A 20050217

• Exploring the dynamics of hydrogen atom release from the radical-radical reaction of O(3P) with C3H5.

  The Journal of chemical physics 20040501

• Density functional theory investigation of the reaction of isodiiodomethane with acetylene: potential utility of isodiiodomethane for cyclopropenation reactions.

  The Journal of organic chemistry 20020628

• Asymmetric synthesis of trans-2,3-piperidinedicarboxylic acid and trans-3,4-piperidinedicarboxylic acid derivatives.

  The Journal of organic chemistry 20020208

• 6-Bromomethyl-4H-1,3-dioxin: a versatile bromomethyl vinyl ketone equivalent for heterocycle and carbocycle construction.

  Journal of the American Chemical Society 20020206

• Polarity of the transition state controls the reactivity of related charged phenyl radicals toward atom and group donors.

  The Journal of organic chemistry 20010420