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N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)triphenylphosphine imide is a complex organic compound that combines a phosphine moiety with a tetra-O-acetylated β-D-glucopyranosyl group. N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)triphenylphosphine imide is characterized by its unique structure, where a triphenylphosphine group is connected to a β-D-glucopyranosyl unit, which is a type of sugar molecule. The tetra-O-acetyl groups protect the hydroxyl groups of the sugar, which is a common strategy in organic synthesis to prevent unwanted side reactions. N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)triphenylphosphine imide is of interest in the field of carbohydrate chemistry and may have potential applications in the synthesis of complex glycoconjugates, which are important in biological systems and医药领域. The specific properties and reactivity of N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)triphenylphosphine imide would depend on the context of its use, such as in the formation of glycosidic bonds or as a protecting group in carbohydrate chemistry.

6919-94-4

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6919-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6919-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6919-94:
(6*6)+(5*9)+(4*1)+(3*9)+(2*9)+(1*4)=134
134 % 10 = 4
So 6919-94-4 is a valid CAS Registry Number.

6919-94-4Downstream Products

6919-94-4Relevant academic research and scientific papers

Cyclometalated gold(III) iminophosphoranes which incorporate carbohydrate groups

Jarman, Bevan P.,Nicholson, Brian K.

, p. 1 - 9 (2012)

Iminophosphoranes with organic groups derived from d-glucose, d-galactose and l-arabinose have been used to prepare gold(III) dichloride complexes via mercurated intermediates, since direct cyclometallation was unsuccessful. Structures and full spectroscopic data are reported. Replacement of one or more of the chloride ligands by PPh3, or by thiosalicylate gave new derivatives. Biological screening showed no enhanced activity relative to other alkyl or aryl analogues.

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