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Methyl-α,β-2,4,6-trideoxy-2,4-di-C-methyl-D-galactopyranoside is a complex organic compound belonging to the class of deoxy sugars. It is a derivative of D-galactopyranoside, a monosaccharide, with three hydroxyl groups removed (trideoxy) and two carbon atoms methylated at the 2nd and 4th positions. This chemical modification results in a unique structure that can have specific biological activities or be used as a building block in the synthesis of more complex molecules. The compound is characterized by its stereochemistry, with the D-configuration indicating the spatial arrangement of hydroxyl groups around the pyranose ring. It is often studied in the context of carbohydrate chemistry and may have applications in pharmaceuticals or materials science due to its potential to interact with biological systems in novel ways.

3720-33-0

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3720-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3720-33-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,2 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3720-33:
(6*3)+(5*7)+(4*2)+(3*0)+(2*3)+(1*3)=70
70 % 10 = 0
So 3720-33-0 is a valid CAS Registry Number.

3720-33-0Downstream Products

3720-33-0Relevant academic research and scientific papers

SYNTHESIS OF MACROLIDE ANTIBIOTICS. 22. SYNTHESIS OF THE C8-C13 FRAGMENT OF OLEANDONOLIDE

Sviridov, A. F.,Yashunskii, D. V.,Kuz'min, A. S.,Kochetkov, N. K.

, p. 1894 - 1900 (2007/10/02)

The stereospecific synthesis of the C8-C13 fragment of oleandonolide was caried out in 15 steps with an overall yield of 4.48percent.

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