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dimethyl ε-truxillate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100100-59-2

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100100-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100100-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,0 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100100-59:
(8*1)+(7*0)+(6*0)+(5*1)+(4*0)+(3*0)+(2*5)+(1*9)=32
32 % 10 = 2
So 100100-59-2 is a valid CAS Registry Number.

100100-59-2Relevant academic research and scientific papers

Lewis Acid Catalysis of Photochemical Reactions. 7. Photodimerization and Cross-Cycloaddition of Cinnamic Esters

Lewis, Frederick D.,Quillen, Suzanne L.,Hale, Paul D.,Oxman, Joe D

, p. 1261 - 1267 (2007/10/02)

The effects of Lewis acid complexation upon the molecular structure, solid-state photodimerization, and solution dimerization and cross-cycloaddition of cinnamic esters have been investigated.Comparison of crystal structures for free and SnCl4-complexed ethyl cinnamate indicates that the enone double bonds are lengthened, the single bonds are shortened, and the enone conformation changes from s-cis to s-trans upon complexation.These changes are consistent with calculated changes in ? bonding and net charges.Solid-state photodimerization of free and complexed cinnamic esters and related molecules yield syn head-to-tail (α-truxillate) dimers.In most cases the Lewis acid complexes dimerize more efficiently and stereoselectively than the free esters.Photodimerization and cross-cycloaddition of methyl cinnamate in dilute solution is also catalyzed by Lewis acids.The mechanism of these reactions involves electronic excitation of a ground-state methyl cinnamate-Lewis acid complex followed by reaction of the excited complex with ground-state ester (dimerization) or simple olefin (cross-cycloaddition).The catalytic effect of Lewis acids is attributed to an increase in excited-state lifetime and reactivity.

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