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Benzoic acid (2S,3S,4R,6R)-6-((2R,3R)-3-benzyloxy-2-hydroxy-5,5,6-trimethyl-4-oxo-hept-6-enyl)-2-bromomethyl-4-methoxy-tetrahydro-pyran-3-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

674769-36-9

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674769-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 674769-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,4,7,6 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 674769-36:
(8*6)+(7*7)+(6*4)+(5*7)+(4*6)+(3*9)+(2*3)+(1*6)=219
219 % 10 = 9
So 674769-36-9 is a valid CAS Registry Number.

674769-36-9Relevant academic research and scientific papers

Synthesis of the C(1)-C(12) segment of peloruside A by an α-benzyloxymethyl ketone aldol strategy

Engers, Darren W.,Bassindale, Martin J.,Pagenkopf, Brian L.

, p. 663 - 666 (2007/10/03)

The C(1)-C(12) segment of 16-membered antitumor macrolide peloruside A has been prepared by a BF3·OEt2-catalyzed Mukaiyama aldol reaction between a glucose-derived C(1)-C(7) aldehyde and a C(8)-C(12) α-benzyloxymethyl ketone. Exclusive 2,3-anti and moderate 3,5-anti/syn facial selectivity (3.5:1) was observed in the aldol reaction. The key C(1)-C(7) aldehyde contains the required stereochemistry at carbons two, three, and five, and has been efficiently prepared on multigram scales from commercial triacetyl D-glucal.

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