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(5R,6R)-5-(tert-butyldiphenylsilyloxy)-6-methyl-7-phenylheptanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

306281-49-2

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306281-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 306281-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,2,8 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 306281-49:
(8*3)+(7*0)+(6*6)+(5*2)+(4*8)+(3*1)+(2*4)+(1*9)=122
122 % 10 = 2
So 306281-49-2 is a valid CAS Registry Number.

306281-49-2Downstream Products

306281-49-2Relevant academic research and scientific papers

Total Synthesis of (+)-Zaragozic Acid C

Armstrong, Alan,Barsanti, Paul A.,Jones, Lyn H.,Ahmed, Ghafoor

, p. 7020 - 7032 (2007/10/03)

A total synthesis of (+)-zaragozic acid C is described. Key features of the synthesis are the use of a double Sharpless asymmetric dihydroxylation reaction of diene 6 to control stereochemistry at four contiguous stereocenters from C3 to C6; the introduction of the C1-side chain by reaction between the anion derived from the dithiane monosulfoxide 27 and the core aldehyde 12; a high yielding, acid-mediated simultaneous acetonide deprotection-dithiane removal-ketalization procedure leading exclusively to the 2,8-dioxabicyclo[3.2.1]octane core 34; and a novel triple oxidation procedure allowing installation of the tricarboxylic acid.

Total synthesis of (+)-zaragozic acid C

Armstrong, Alan,Jones, Lyn H.,Barsanti, Paul A.

, p. 3337 - 3340 (2007/10/03)

A total synthesis of (+)-zaragozic acid C is described. Key steps are an acid-mediated acetonide deprotection-dithiane removal-ketalisation procedure, providing selectively the 2,8-dioxabicyclo[3.2.1]octane core of the natural product, and the simultaneou

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