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2-Propanone, 1-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-3-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

335393-68-5

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335393-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 335393-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,3,9 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 335393-68:
(8*3)+(7*3)+(6*5)+(5*3)+(4*9)+(3*3)+(2*6)+(1*8)=155
155 % 10 = 5
So 335393-68-5 is a valid CAS Registry Number.

335393-68-5Downstream Products

335393-68-5Relevant articles and documents

Diastereoselective synthesis of vicinal tertiary diols

Loertscher, Brad M.,Young, Phil R.,Evans, Patrick R.,Castle, Steven L.

supporting information, p. 1930 - 1933 (2013/06/05)

A strategy for the synthesis of differentiated vicinal tertiary diols is described. The key step is a high-yielding, diastereoselective LaCl 3·2LiCl-mediated addition of a Grignard or organolithium reagent to ketone 2a. The reaction is believed to proceed via a 1,3-chelated intermediate. One of the adducts has been transformed into a functionalized cyclopentenone resembling the core structure of pactamycin.

Conformationally Constrained Analogues of Diacylglycerol. 20. The Search for an Elusive Binding Site on Protein Kinase C through Relocation of the Carbonyl Pharmacophore Along the sn-1 Side Chain of 1,2-Diacylglycerol Lactones

Tamamura, Hirokazu,Sigano, Dina M.,Lewin, Nancy E.,Blumberg, Peter M.,Marquez, Victor E.

, p. 644 - 655 (2007/10/03)

Previous studies with 1,2-diacylglycerol (DAG) lactones, which behave as high-affinity ligands for protein kinase C (PK-C), have established the importance of maintaining intact the pharmacophore triad of two carbonyl moieties (sn-1 and sn-2) and the prim

A new synthetic route towards the mono-O-protected anti-conformationally constrained pyrimidine acyclic nucleoside.

Liu, Chi-Tsan,Tu, Tsu-Chiang,Hsu, Ling-Yih

, p. 1028 - 1030 (2007/10/03)

Novel synthetic approach to mono-O-protected anti-conformationally constrained pyrimidine acyclic nucleoside was attained from the coupling of lithiated 2,4-dimethoxy-6-methylpyrimidine with 1-benzyloxy-3-(tert-butyldiphenylsilyloxy)propan-2-one, followed by the sequential reactions of methylthiomethylation, cyclization, hydroxylation, and dealkylation.

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