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D-Digitoxose Tribenzoate is a derivative of D-ribo-Hexonic acid, which is metabolized in the liver. It is an off-white solid and has the chemical formula C24H26O12. D-Digitoxose Tribenzoate inhibits glucose-stimulated insulin release, making it a potential candidate for pharmaceutical applications.

104652-04-2

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104652-04-2 Usage

Uses

Used in Pharmaceutical Industry:
D-Digitoxose Tribenzoate is used as a pharmaceutical agent for its ability to inhibit glucose-stimulated insulin release. This property makes it a promising candidate for the development of drugs targeting diabetes and related metabolic disorders.
Used in Drug Development:
D-Digitoxose Tribenzoate is used in drug development as a starting material or intermediate for the synthesis of other bioactive compounds. Its unique chemical properties and inhibitory effects on insulin release can be leveraged to create novel therapeutic agents for various diseases.
Used in Research:
D-Digitoxose Tribenzoate is used as a research tool in the study of glucose metabolism, insulin release, and related cellular processes. It can help researchers gain insights into the mechanisms underlying diabetes and other metabolic disorders, potentially leading to the discovery of new treatments and interventions.

Check Digit Verification of cas no

The CAS Registry Mumber 104652-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,5 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104652-04:
(8*1)+(7*0)+(6*4)+(5*6)+(4*5)+(3*2)+(2*0)+(1*4)=92
92 % 10 = 2
So 104652-04-2 is a valid CAS Registry Number.

104652-04-2Relevant academic research and scientific papers

Syntheses of Selectively Alkylated Enol Ethers in the L-ribo Series

Koepper, Sabine,Lundt, Inge,Pedersen, Christian,Thiem, Joachim

, p. 531 - 536 (2007/10/02)

The reduction of enulose 1a predominantly leads to L-digitoxal (3a), although this method presents a sluggish reaction with moderate yields.In contrast, the preparation from L-digitoxose (4a) in a three-step one-pot procedure represents an advantageous approach.Regioselective 3- or 4-O-alkylations are achieved by phase-transfer catalysis method or via stannylidene intermediates to give monosaccharide precursors of the L-ribo series valuable for further interglycosidic linking.

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