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α1-deoxy-1-(C-2',4'-dimethoxyphenyl)-2,3,4,6-tetra-O-benzyl-D-glucopyranose is a complex organic compound that belongs to the class of carbohydrates, specifically a derivative of D-glucose. This molecule features a unique structure where the aldehyde group at the first carbon (C1) is reduced to a hydroxyl group, making it a deoxy sugar. The molecule is further characterized by the presence of a 2',4'-dimethoxyphenyl group attached to the first carbon, which introduces additional methoxy substituents at the 2' and 4' positions of the phenyl ring. Additionally, the 2nd, 3rd, 4th, and 6th carbons of the glucopyranose ring are each protected with a benzyl group, which is a common strategy in organic synthesis to prevent unwanted side reactions and to facilitate the selective modification of specific functional groups. α1-deoxy-1-(C-2',4'-dimethoxyphenyl)-2,3,4,6-tetra-O-benzyl-D-glucopyranose is of interest in the field of organic chemistry, particularly in the synthesis of complex natural products and the development of new pharmaceuticals, due to its potential to serve as a building block or intermediate in the construction of more elaborate molecular structures.

96689-84-8

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96689-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96689-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,6,8 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96689-84:
(7*9)+(6*6)+(5*6)+(4*8)+(3*9)+(2*8)+(1*4)=208
208 % 10 = 8
So 96689-84-8 is a valid CAS Registry Number.

96689-84-8Relevant academic research and scientific papers

2′-Carboxybenzyl glycosides: glycosyl donors for C-glycosylation and conversion into other glycosyl donors

Lee, Yong Joo,Baek, Ju Yuel,Lee, Bo-Young,Kang, Sung Soo,Park, Hye-Seo,Jeon, Heung Bae,Kim, Kwan Soo

, p. 1708 - 1716 (2007/10/03)

Glycosylation of various glycosyl acceptors with 2′-carboxybenzyl (CB) 2,3,4,6-tetra-O-benzyl-β-d-glucopyranoside and CB 2,3,4,6-tetra-O-benzyl-α-d-mannopyranoside as glycosyl donors afforded α-C-glycosides exclusively or predominantly in good yields. CB

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-Glycosylflavonoids, I. - Synthesis of 4',7-Di-O-methylisobayin

Tschesche, Rudolf,Widera, Wolfgang

, p. 902 - 907 (2007/10/02)

Reaction of 2,4-dimethoxyphenylmagnesium bromide with 2,3,4,6-tetra-O-benzylglucopyranosyl chloride in THF gave mainly 2,3,4,6-tetra-O-benzyl-1-(2,4-dimethoxyphenyl)-1-desoxy-β-D-glucopyranose (1).After cleavage of the benzyl groups and acetylation the te

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