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(2R,3S,4S,6S)-4-benzyloxy-7-(tert-butyldiphenylsiloxy)-2,6-dimethyl-5-methoxymethoxyheptanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

623938-88-5

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623938-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 623938-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,9,3 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 623938-88:
(8*6)+(7*2)+(6*3)+(5*9)+(4*3)+(3*8)+(2*8)+(1*8)=185
185 % 10 = 5
So 623938-88-5 is a valid CAS Registry Number.

623938-88-5Downstream Products

623938-88-5Relevant academic research and scientific papers

Polymer-Supported Bisacetoxybromate(I) Anion - An Efficient Co-Oxidant in the TEMPO-Mediated Oxidation of Primary and Secondary Alcohols

Bruenjes, Marco,Sourkouni-Argirusi, Georgia,Kirschning, Andreas

, p. 635 - 642 (2003)

A polymer-bound reagent for the efficient oxidation of primary alcohols to aldehydes and secondary alcohols to ketones in the presence of a catalytic amount of 2,2,6,6-tetramethyl-1-piperidinyloxyl (TEMPO) is described. The oxidation process is particular mild and allows one to prepare aldehydes with α-chirality without racemization. This also includes the synthesis of α-aminoaldehydes. In most cases, work-up of this heavy metal-free oxidation is achieved by simple filtration followed by removal of the solvent. Insight into the role of the bromate(I) anion in the oxidation process was gained from the TEMPO-mediated oxidation of benzaldehyde in the presence of the hypochlorite anion loaded on an anion exchange resin.

Towards the total synthesis of tonantzitlolone - Preparation of key fragments and the complete carbon backbone

Wittenberg, Rüdiger,Beier, Christian,Dr?ger, Gerald,Jas, Gerhard,Jasper, Christian,Monenschein, Holger,Kirschning, Andreas

, p. 4457 - 4460 (2007/10/03)

The first synthetic advances towards the novel diterpenoid tonantzitlolone 1 are described. The key steps in the synthesis involve a chromium(II) Reformatsky reaction, a diastereoselective C1 extension and an expeditious aldol coupling step of

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