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Benzoic acid, 3-(phenylmethoxy)-5-(2-propenyloxy)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

497069-05-3

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497069-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497069-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,0,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 497069-05:
(8*4)+(7*9)+(6*7)+(5*0)+(4*6)+(3*9)+(2*0)+(1*5)=193
193 % 10 = 3
So 497069-05-3 is a valid CAS Registry Number.

497069-05-3Relevant academic research and scientific papers

Sequences in Dendrons and Dendrimers

Sivanandan, Kulandaivelu,Sandanaraj, Britto S.,Thayumanavan

, p. 2937 - 2944 (2007/10/03)

Sequential incorporation of a variety of functional groups forms the basis for specificity in biomacromolecules. Introduction of such diversity and sequencing ability in artificial macromolecules is fundamentally interesting. In this paper, three different synthetic approaches have been used to build dendrons and dendrimers in which all the monomer units are different from each other. The synthetic strategies described in this paper involve the use of (i) an ABBp monomer, (ii) an ABB′ monomer, and (iii) an ABB m monomer. The complementarity and the versatility of these synthetic approaches should render them useful for a variety of applications.

A mild deprotection strategy for allyl-protecting groups and its implications in sequence specific dendrimer synthesis

Vutukuri, Dharma Rao,Bharathi, Pandi,Yu, Zhouying,Rajasekaran, Karthik,Tran, My-Huyen,Thayumanavan

, p. 1146 - 1149 (2007/10/03)

A mild deprotection strategy for allyl ethers under basic conditions in the presence of a palladium catalyst is described. Under these conditions, aryl allyl ethers can be cleaved selectively in the presence of alkyl allyl ethers. These conditions are also effective in the deprotection of allyloxycarbonyl groups. The utility of the current methodology in sequence specific dendrimer synthesis is demonstrated.

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