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2,2,6,6-Tetramethylpiperidin-4-yl tetra-O-benzyl-α-D-galactopyranoside hydrochloride is a complex organic compound that serves as a protecting group in carbohydrate chemistry. It is a derivative of α-D-galactopyranoside, a monosaccharide, with four benzyl groups attached to the hydroxyl groups at the 2, 3, 4, and 6 positions. The tetramethylpiperidin-4-yl group is attached to the nitrogen atom, and the compound is further modified with a hydrochloride ion. This structure is used to protect the galactopyranoside moiety during chemical reactions, preventing unwanted side reactions and ensuring the selective modification of other functional groups. The hydrochloride salt form enhances the solubility and stability of the compound in various solvents, making it a valuable tool in the synthesis of complex carbohydrates and related bioactive molecules.

77895-15-9

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77895-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77895-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,9 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77895-15:
(7*7)+(6*7)+(5*8)+(4*9)+(3*5)+(2*1)+(1*5)=189
189 % 10 = 9
So 77895-15-9 is a valid CAS Registry Number.

77895-15-9Downstream Products

77895-15-9Relevant academic research and scientific papers

Synthesis of alpha- and beta-glycosides containing spin labels, as probes for studies of carbohydrate-protein interaction.

Plessas,Goldstein

, p. 211 - 220 (2007/10/02)

Nitroxide spin-labeled alpha-D-glycopyranosides were synthesized in good yield and in a highly stereoselective manner by reaction of per-O-benzyl-alpha-D-glycopyranosyl bromides with 2,2,6,6-tetramethyl-4-piperidinol under the bromide ion-catalyzed conditions devised by Lemieux et al. After hydrogenolysis, the deblocked intermediates were oxidized to give the desired, spin-labeled alpha-D-glycopyranosides. Nitroxide spin-labeled beta-D-glycopyranosides, as well as a beta-maltoside, were synthesized by standard methods. The synthesis is also described of 2-amino-2-deoxy-D-glucose and -D-galactose derivatives having a spin label at C-2, and of the spin-labeled compound 1-[4-(beta-D-galactopyranosyloxy)phenyl]-3-(2,2,6,6-tetramethylpiperidin-1-oxyl -4-yl)-2-thiourea.

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