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β-D-glucopyranosyl-2,4,6-trimethoxybenzene is a complex organic compound consisting of a benzene ring with three methoxy groups attached at the 2, 4, and 6 positions, and a β-D-glucopyranosyl moiety linked to the benzene ring. β-D-glucopyranosyl-2,4,6-trimethoxybenzene is a type of glycoside, where a sugar molecule (in this case, β-D-glucose) is bonded to a non-carbohydrate molecule (the benzene ring). The presence of the methoxy groups and the glucose unit gives β-D-glucopyranosyl-2,4,6-trimethoxybenzene unique chemical and biological properties, which may have potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. The specific structure and functional groups of β-D-glucopyranosyl-2,4,6-trimethoxybenzene contribute to its reactivity, solubility, and potential interactions with other molecules, making it an interesting subject for further research and development.

89648-16-8

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89648-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89648-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,4 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89648-16:
(7*8)+(6*9)+(5*6)+(4*4)+(3*8)+(2*1)+(1*6)=188
188 % 10 = 8
So 89648-16-8 is a valid CAS Registry Number.

89648-16-8Relevant academic research and scientific papers

Carbocyclic ring closure of unsaturated S-, Se-, and C-aryl glycosides

Sollogoub, Matthieu,Mallet, Jean-Maurice,Sinay, Pierre

, p. 362 - 364 (2000)

Triisobutylaluminum-promoted rearrangement of unsaturated glycosides containing electron-donating aglycons - such as C-aryl glycoside 1, or O-, S- , and Seglycosides - provides direct access to highly functionalized cyclohexane derivatives such as 2.

Triisobutylaluminium (TIBAL) promoted rearrangement of C-glycosides

Sollogoub, Matthieu,Sinay, Pierre

, p. 843 - 858 (2007/10/03)

Triisobutylaluminium-promoted rearrangement of unsaturated glycosides containing electron-donating aglycons, such as C-aryl glycosides, provides direct access to highly functionalised cyclohexane derivatives.

C-GLYCOSIDATION OF PYRIDYL THIOGLYCOSIDES

Williams, Robert M.,Stewart, Andrew O.

, p. 2715 - 2718 (2007/10/02)

The pyridylthioglycosides 1 are efficiently transformed into the corresponding C-glycosides via reaction with silver(I) triflate and a variety of carbon nucleophiles.

C-GLYCOSIDES FROM O-GLYCOSYL TRICHLOROACETIMIDATES

Schmidt, Richard R.,Hoffmann, Michael

, p. 409 - 412 (2007/10/02)

From O-glycosyl trichloroacetimidates 2, 9, and 13 and activated benzene derivatives C-aryl glycosides were obtained by mild Lewis acid catalysis.In most cases only one stereoisomer was formed, however, the α-alkoxyalkyl transfer took place not always by

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