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(Z)-methyl 2-bromomethyl-3-dimethyl(phenyl)silylprop-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145745-77-3

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145745-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145745-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,7,4 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 145745-77:
(8*1)+(7*4)+(6*5)+(5*7)+(4*4)+(3*5)+(2*7)+(1*7)=153
153 % 10 = 3
So 145745-77-3 is a valid CAS Registry Number.

145745-77-3Downstream Products

145745-77-3Relevant academic research and scientific papers

The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow

Roper, Kimberley A.,Berry, Malcolm B.,Ley, Steven V.

, p. 1781 - 1790 (2013)

The application of a monolithic form of triphenylphosphine to the Ramirez gem-dibromoolefination reaction using flow chemistry techniques is reported. A variety of gem-dibromides were synthesised in high purity and excellent yield following only removal of solvent and no further off-line purification. It is also possible to perform the Appel reaction using the same monolith and the relationship between the mechanisms of the two reactions is discussed.

Chemistry of Insect Antifeedants from Azadirachta indica (Part 12): Use of Silicon as a Control Element in the Synthesis of a Highly Functionalized Decalin Fragment of Azadirachtin

Kolb, Hartmuth C.,Ley, Steven V.,Slawin, Alexandra M. Z.,Williams, David J.

, p. 2735 - 2762 (2007/10/02)

A diastereoselective synthesis of a highly functionalized decalin fragment 61 of the insect antifeedant azadirachtin 1 is described.An intramolecular Diels-Alder reaction of triene 15 and subsequent intramolecular aldol reaction were employed to assemble

Chemistry of insect antifeedants from Azadirachta Indica (Part 10): Synthesis of a highly functionalised decalin fragment of azadirachtin

Kolb,Ley

, p. 6187 - 6190 (2007/10/02)

The synthesis of a highly functionalised decalin fragment (2) of the antifeedant azadirachtin (1) is described. A silyl group was employed to control the stereoselectivity of several key steps and to introduce C3 hydroxyl functionality. A novel ring contr

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