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(E)-1-chloro-4-methyl-hept-3,6-diene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127679-03-2

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127679-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127679-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,7 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127679-03:
(8*1)+(7*2)+(6*7)+(5*6)+(4*7)+(3*9)+(2*0)+(1*3)=152
152 % 10 = 2
So 127679-03-2 is a valid CAS Registry Number.

127679-03-2Downstream Products

127679-03-2Relevant articles and documents

Etude de la reactivite de l'allyltrimethylsilane avec les cetones α-cyclopropaniques en presence de tetrachlorure de titane

Monti, Honore,Afshari, Mohammad,Leandri, Gilbert

, p. 69 - 78 (2007/10/02)

The reaction of diversely substituted α-cyclopropylketones with allyltrimethylsilane in the presence of titanium tetrachloride has been studied.The products formation is explained by the intervention of a cyclopropylcarbinyl transient cation formed after a first 1,2-addition on the carbonyl.With regard to the structure of the starting compounds, this intermediate reacts with a second molecule of allylsilane, either by a bimolecular addition on the carbocycle, or by the direct attack on the carbon bearing the formal positive charge yielding diallyl and functionalisedcyclohexane derivatives.A general mechanism is proposed.Keywords: Silicon; Titanium; Allyltrimethylsilane; Lewis acids; Reaction mechanism

Reactivite de l'allyltrimethylsilane avec les acetylcyclopropanes en presence d'acide de Lewis

Piras, P.,Afshari, M.,Leandri, G.,Monti, H.

, p. C9 - C11 (2007/10/02)

In the presence of Lewis acid, allyltrimethylsilane undergoes 1,2-addition to the carbonyl system of acetylcyclopropanes.A second direct attack of the nucleophilic reagent on the transient cyclopropylcarbynyl cation formed yields diallylic and functionalised cyclohexane derivatives.

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