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chlorotris(((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)oxy)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18765-53-2

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18765-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18765-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,6 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18765-53:
(7*1)+(6*8)+(5*7)+(4*6)+(3*5)+(2*5)+(1*3)=142
142 % 10 = 2
So 18765-53-2 is a valid CAS Registry Number.

18765-53-2Relevant academic research and scientific papers

Chiral trialkoxysilanols derived from terpene alcohols. Molecular structures of tris([(1S)-endo]-(-)-bornoxy)silanol and tetrakis((-)-menthoxy)silane

Beckmann, Jens,Dakternieks, Dainis,Tiekink, Edward R.T

, p. 188 - 192 (2002)

Terpene alcohols (-)-menthol and [(1S)-endo]-(-)-borneol react with SiCl4 in the presence of base to give (MenO)3SiCl (1) and (BorO)3SiCl (2) in high yields. Hydrolysis of 1 yields (MenO)3SiOH (4) and (MenO)sub

Silicate esters of paclitaxel and docetaxel: Synthesis, hydrophobicity, hydrolytic stability, cytotoxicity, and prodrug potential

Wohl, Adam R.,Michel, Andrew R.,Kalscheuer, Stephen,Macosko, Christopher W.,Panyam, Jayanth,Hoye, Thomas R.

, p. 2368 - 2379 (2014/04/17)

We report here the synthesis and selected properties of various silicate ester derivatives (tetraalkoxysilanes) of the taxanes paclitaxel (PTX) and docetaxel (DTX) [i.e., PTX-OSi(OR)3 and DTX-OSi(OR)3]. Both the hydrophobicity and hydrolytic lability of these silicates can be (independently) controlled by choice of the alkyl group (R). The synthesis, structural characterization, hydrolytic reactivity, and in vitro cytotoxicity against the MDA-MB-231 breast cancer cell line of most of these derivatives are described. We envision that the greater hydrophobicity of these silicates (vis-à-vis PTX or DTX itself) should be advantageous from the perspective of preparation of stable aqueous dispersions of amphiphilic block-copolymer-based nanoparticle formulations.

The First Tri- and Tetraalkoxysilanes with Four Different Substituents

Clausen, Rasmus P.,Bols, Mikael

, p. 4457 - 4464 (2007/10/03)

Unsymmetrically substituted tri- and tetraalkoxysilanes were surprisingly found to be configurationally stable and easy to prepare. It was found that compounds of type MeSi(OR)2(OR′), MeSi- (OR)(OR′)(OR″), Si(OR)2(OR′)2, Si(OR)2(OR′)(OR″), Si(OR)3(OR′), and even Si(OR)(OR′)(OR″)(OR*) could be obtained by sequential addition of a variety of chiral and achiral alcohols to methyltrichlorosilane or tetrachlorosilane in the presence of pyridine. In the case of MeSi(OR)(OR′)(OR″) and Si(OR)(OR′)(OR″)(OR*), two types of compounds that have never been prepared before, were obtained in good yield.

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