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(2R,3R)-3-(Benzoyloxy)-2,3-dihydro-2,3-dimethoxy-6-methyl-4H-pyran-4-one is a complex organic compound with a molecular formula of C16H18O6. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of compounds known as pyranones. This specific compound features a pyran ring system with a 4-oxo group, which is part of the larger family of heterocyclic compounds. The molecule is characterized by the presence of two methoxy groups at the 2 and 3 positions, a benzoyloxy group at the 3 position, and a methyl group at the 6 position. The compound is synthesized as a racemic mixture, with the R configuration at both the 2 and 3 positions. It is used in the synthesis of various pharmaceuticals and natural products due to its unique structural features and reactivity.

72076-12-1

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72076-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72076-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,7 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72076-12:
(7*7)+(6*2)+(5*0)+(4*7)+(3*6)+(2*1)+(1*2)=111
111 % 10 = 1
So 72076-12-1 is a valid CAS Registry Number.

72076-12-1Downstream Products

72076-12-1Relevant academic research and scientific papers

Enantiomerically Pure Building Blocks from Sugars, 10 2,3-Dihydropyranones with Contiguous Chiral Centers: Practical Routes for Their Aquisition and Evaluation of their Reaction Potential

Lichtenthaler, Frieder W.,Nishiyama, Shigeru,Weimer, Thomas

, p. 1163 - 1170 (2007/10/02)

A practical, large-scale adaptable four-step procedure has been developed for the conversion of D-glucose into pyranoid enediolone esters with (R,R)-configuration in contiguous chiral centers, involving hydrolysis of the readily accessible bis-acetonide o

ANOMERIC STEREOCONTROL IN ADDITION REACTIONS TO HEXOSE-DERIVED DIHYDROPYRANONES

Lichtenthaler, Frieder W.,Nishiyama, Shigeru,Koehler, Peter,Lindner, Hans J.

, p. 13 - 26 (2007/10/02)

The outcome of base-catalysed O- and C-nucleophile additions to the carbonyl group of benzoylated 4-deoxy-D-glycero-hex-3-enopyranosid-2-ulose (1) depends on the conditions used.With methanol / sodium iodide, methanol / sodium methoxide (traces), or methy

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