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2,3-Diacetamido-1,4,5,6-tetra-O-acetyl-2,3-didesoxy-muco-inosit is a complex organic compound with the molecular formula C20H27NO13. It is a derivative of inositol, a sugar alcohol that plays a crucial role in various biological processes, including signal transduction and lipid metabolism. This specific compound features two acetamido groups at the 2 and 3 positions, and four acetyl groups attached to the hydroxyl groups at the 1, 4, 5, and 6 positions. The term "2,3-didesoxy" indicates the absence of two oxygen atoms at the 2 and 3 positions, which is a modification of the parent inositol structure. 2,3-Diacetamido-1,4,5,6-tetra-O-acetyl-2,3-didesoxy-muco-inosit is of interest in chemical and pharmaceutical research due to its potential applications in the development of drugs targeting inositol-related pathways.

6730-23-0

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6730-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6730-23-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,3 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6730-23:
(6*6)+(5*7)+(4*3)+(3*0)+(2*2)+(1*3)=90
90 % 10 = 0
So 6730-23-0 is a valid CAS Registry Number.

6730-23-0Downstream Products

6730-23-0Relevant academic research and scientific papers

Polyhydroxyamino Compounds via Diene Synthesis with Nitroso Compounds, IX. - trans-6-Azido-1,3-cyclohexadien-5-ol as Educt for the Synthesis of Kondurodiamine and Streptamine Isomers

Kresze, Guenter,Weiss, Martha M.,Dittel, Werner

, p. 203 - 212 (2007/10/02)

The diaminodideoxykonduritols 8a, 8b, and 9 as well as the analogs 10 and 11 of Streptamine have been synthesized starting with O,N-5,6-disubstituted cyclohexadienes.

Polyhydroxyamino Compounds via Diene Synthesis with Nitroso Compounds, VIII. - Preparation of Diamino Derivatives via Epoxides

Kresze, Guenter,Melzer, Horst

, p. 1874 - 1879 (2007/10/02)

The epoxidation of the aminocyclohexenols 1 proceeds specifically with syn-attack and formation of the epoxides 2.Reactions of 2 with ammonia or dimethylamine leads to the inosdiamines 3 or 4, respectively.

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