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N-(2-phenylethylaminocarbonyl)-β-D-glucopyranosylamine is a complex organic compound that combines a phenylethylamine moiety with a β-D-glucopyranosylamine group. This molecule features a phenyl ring attached to an ethylamine chain, which is then connected to a glucopyranosylamine unit through a carbonyl linker. The β-D-glucopyranosylamine part of the molecule is a derivative of glucose, with an amine group replacing one of the hydroxyl groups. This chemical structure is significant in the field of carbohydrate chemistry and may have applications in the synthesis of pharmaceuticals or other bioactive compounds due to its potential to interact with biological systems. The specific arrangement of the phenylethylamine and the glucopyranosylamine parts can influence the molecule's reactivity and its ability to form complexes with proteins or other biomolecules, making it a subject of interest for researchers in medicinal chemistry and related fields.

4490-93-1

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4490-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4490-93-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,9 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4490-93:
(6*4)+(5*4)+(4*9)+(3*0)+(2*9)+(1*3)=101
101 % 10 = 1
So 4490-93-1 is a valid CAS Registry Number.

4490-93-1Downstream Products

4490-93-1Relevant academic research and scientific papers

Protecting group free synthesis of urea-linked glycoconjugates: Efficient synthesis of β-urea glycosides in aqueous solution

Ichikawa, Yoshiyasu,Minami, Takahiro,Kusaba, Shohei,Saeki, Nobuyoshi,Tonegawa, Yuta,Tomita, Yumiko,Nakano, Keiji,Kotsuki, Hiyoshizo,Masuda, Toshiya

supporting information, p. 3924 - 3931 (2014/06/09)

A method for the protecting group free synthesis of β-urea-linked glycoconjugates has been developed. The one step process, involving reactions between urea and d-glucose, N-acetyl-d-glucosamine or d-xylose in acidic aqueous solution, furnishes the corresponding β-urea glycosides in modest yields. This simple and efficient procedure is applicable to the synthesis of β-urea tethered amino acid-carbohydrate conjugates. This journal is the Partner Organisations 2014.

Synthesis of urea-tethered neoglycoconjugates and pseudooligosaccharides in water

Ichikawa, Yoshiyasu,Matsukawa, Yohei,Isobe, Minoru

, p. 3934 - 3938 (2007/10/03)

A novel approach to the synthesis of urea glycosides in aqueous media has been explored. Steyermark's glucopyranosyl oxazolidinone was found to be a good synthon for anchoring glucosyl moieties onto amines and thiols. The present method was successfully a

Urea glycoside synthesis in water

Ichikawa, Yoshiyasu,Matsukawa, Yohei,Isobe, Minoru

, p. 1019 - 1022 (2007/10/03)

A novel approach to the synthesis of urea glycosides in aqueous media has been developed. Reaction of Steyermark's glucosyl carbamate 1 with amines was carried out in water to afford urea glucosides in good yields. This method was successfully applied to

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