85281-06-7 Usage
Uses
Used in Medicinal Chemistry:
2-Oxa-4-azabicyclo[3.3.1]nonan-3-one,6,7,8-trihydroxy-1-(hydroxymethyl)-, is used as a potential active pharmaceutical ingredient for the development of new drugs due to its unique structure and multiple functional groups that can interact with biological targets.
Used in Drug Discovery:
In the field of drug discovery, 2-Oxa-4-azabicyclo[3.3.1]nonan-3-one,6,7,8-trihydroxy-1-(hydroxymethyl)-, is utilized as a lead compound for the identification and optimization of new therapeutic agents, given its capacity to form various interactions with biological molecules.
Used in Materials Science:
2-Oxa-4-azabicyclo[3.3.1]nonan-3-one,6,7,8-trihydroxy-1-(hydroxymethyl)-, is employed as a component in the development of novel materials, such as polymers or composites, owing to its ability to participate in chemical reactions and form stable structures.
Used in Chemical Research:
In chemical research, 2-Oxa-4-azabicyclo[3.3.1]nonan-3-one,6,7,8-trihydroxy-1-(hydroxymethyl)-, serves as a subject of study to understand its reactivity, stability, and the mechanisms of its interactions with other molecules, which can provide insights into new chemical processes and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 85281-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,8 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85281-06:
(7*8)+(6*5)+(5*2)+(4*8)+(3*1)+(2*0)+(1*6)=137
137 % 10 = 7
So 85281-06-7 is a valid CAS Registry Number.
85281-06-7Relevant academic research and scientific papers
PROCESSES FOR PREPARING 6,7,8-TRIHYDROXY-1-(HYDROXYMETHYL)-3-OXO-2-OXA-4-AZABICYCLO[3.3.1]NONANE
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Page/Page column 6, (2008/06/13)
Provided are processes for preparing 6,7,8-trihydroxy-1-(hydroxymethyl)-3-oxo-2-oxa-4-azabicyclo[3.3.1]nonane and processes for preparing valiolamine or its derivative using the same.
STEREOSELECTIVE CONVERSION OF VALIENAMINE AND VALIDAMINE INTO VALIOLAMINE
Horii, Satoshi,Fukase, Hiroshi,Kameda, Yukihiko
, p. 185 - 200 (2007/10/02)
Methods are described for the stereoselective conversion of valienamine (2) and validamine (3) into valiolamine (1a), a new pseudo-amino sugar isolated from the fermentation broth of Streptomyces hygroscopicus subsp. limoneus and which is a stronger α-D-glucosidase inhibitor than 2 and 3.Treatment of the acyclic carbamates (4) of 2 with halogenation reagents led to ring closure to afford the halo cyclic carbamates (6), which were reductively dehalogenated and then hydrolyzed to give 1a.Similar treatment of the exomethylene acyclic carbamate (12), derived from 3 via 8-11, resulted in the formation of halo cyclic carbamates (14a,b), which were converted into 1a.The synthesis of epivaliolamine (1b), the C-1 epimer of 1a, starting from 2 and 3, is also described.
