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55976-13-1

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55976-13-1 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 107, p. 972, 1985 DOI: 10.1021/ja00290a037Synthesis, p. 658, 1974 DOI: 10.1055/s-1974-23393

Check Digit Verification of cas no

The CAS Registry Mumber 55976-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,7 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55976-13:
(7*5)+(6*5)+(5*9)+(4*7)+(3*6)+(2*1)+(1*3)=161
161 % 10 = 1
So 55976-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H20/c1-3-5-7-9-11-10-8-6-4-2/h3,7,9H,1,4-6,8,10-11H2,2H3/b9-7+

55976-13-1Relevant articles and documents

Novel type of carbozirconation reaction of alkynes

Suzuki, Noriyuki,Kondakov, Denis Y.,Kageyama, Motohiro,Kotora, Martin,Hara, Ryuichiro,Takahashi, Tamotsu

, p. 4519 - 4540 (1995)

Novel type of carbozirconation reaction of alkynes is reported. Treatment of zirconocenealkyne complexes, zirconacyclopentenes, or zirconacyclopentadienes with allylic compounds gave allylzirconation products of alkynes. Carbozirconation of alkynes with zirconacyclopentenes or zirconacyclopentadienes involved β,β'-C-C bond cleavage reaction of zirconacycles. Reactions of zirconacyclopentenes with homoallyl bromides afforded allylcyclopropane derivatives as carbozirconation products.

Engaging Alkenyl Halides with Alkylsilicates via Photoredox Dual Catalysis

Patel, Niki R.,Kelly, Christopher B.,Jouffroy, Matthieu,Molander, Gary A.

supporting information, p. 764 - 767 (2016/03/01)

Single-electron transmetalation via photoredox/nickel dual catalysis provides the opportunity for the construction of Csp3-Csp2 bonds through the transfer of alkyl radicals under very mild reaction conditions. A general procedure for the cross-coupling of primary and secondary (bis-catecholato)alkylsilicates with alkenyl halides is presented. The developed method allows not only alkenyl bromides and iodides but also previously underexplored alkenyl chlorides to be employed. (Chemical Equation Presented).

Reduction of acetylenic compounds to (E)-olefins by alkali metals - An investigation of the scope

Brandsma, Lambert,Nieuwenhuizen, Willem F.,Zwikker, Jan W.,Maeeorg, Uno

, p. 775 - 779 (2007/10/03)

Efficient procedures have been developed for the stereospecific reduction by alkali metals of disubstituted acetylenes with long carbon chains. Acetylenes containing two or more (isolated) triple bonds are reduced considerably more easily than are monoyne

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