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2-O-allyl-1,3-benzylideneglycerol is a complex organic compound with the molecular formula C17H18O3. It is a derivative of glycerol, where the hydroxyl group at the 2-position is substituted with an allyl group, and the hydroxyl groups at the 1 and 3 positions are connected through a benzylidene bridge. 2-O-allyl-1,3-benzylideneglycerol is of interest in the field of organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and other chemical products due to its unique structure. The allyl and benzylidene moieties can participate in a range of chemical reactions, making 2-O-allyl-1,3-benzylideneglycerol a versatile building block for further chemical modifications.

6543-12-0

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6543-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6543-12-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6543-12:
(6*6)+(5*5)+(4*4)+(3*3)+(2*1)+(1*2)=90
90 % 10 = 0
So 6543-12-0 is a valid CAS Registry Number.

6543-12-0Relevant academic research and scientific papers

Original synthesis of linear, branched and cyclic oligoglycerol standards

Cassel, Stephanie,Debaig, Catherine,Benvegnu, Thierry,Chaimbault, Patrick,Lafosse, Michel,Plusquellec, Daniel,Rollin, Patrick

, p. 875 - 896 (2007/10/03)

A variety of authentic standards of linear, branched and cyclic oligomers of glycerol, with well-defined structures and degrees of polymerisation from 2 to 5, have been efficiently synthesised. Linear oligomers were obtained by means of a convergent approach based on regioselective opening of bis(epoxides) with solketal; branched compounds were synthesised using oxidative cleavage of the corresponding anhydrohexitols as the key step. A 6-exo-trig halocyclisation reaction involving heteroatom-tethered unsaturated alcohols permitted an efficient synthesis of the precursors of selected cyclic dimers; larger cyclic oligomers were prepared by two one-pot Williamson reactions using a ditriflate derived from diglycerol. All these methodologies permitted further scaling up.

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