165874-29-3 Usage
Uses
Used in Pharmaceutical Industry:
.beta.-D-Allopyranose, 2-deoxy-4-O-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-.beta.-D-allopyranosyl-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)-, 1-(2,2,2-trichloroethanimidate) is used as a potential therapeutic agent for the development of novel drugs targeting various diseases. .beta.-D-Allopyranose, 2-deoxy-4-O-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-.beta.-D-allopyranosyl-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)-, 1-(2,2,2-trichloroethanimidate)'s unique structure and functional groups may allow for specific interactions with biological targets, potentially leading to the discovery of new treatments for a range of medical conditions.
Used in Research and Development:
In the field of research and development, .beta.-D-Allopyranose, 2-deoxy-4-O-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-.beta.-D-allopyranosyl-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)-, 1-(2,2,2-trichloroethanimidate) can be employed as a starting material or a probe for studying the interactions between carbohydrates and biological systems. This may contribute to a better understanding of carbohydrate biology and the development of new strategies for targeting carbohydrate-related diseases.
Used in Drug Delivery Systems:
.beta.-D-Allopyranose, 2-deoxy-4-O-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-.beta.-D-allopyranosyl-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)-, 1-(2,2,2-trichloroethanimidate) .beta.-D-Allopyranose, 2-deoxy-4-O-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-.beta.-D-allopyranosyl-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)-, 1-(2,2,2-trichloroethanimidate) may also be utilized in the design and development of drug delivery systems. Its unique structure and functional groups could be exploited to enhance the delivery, bioavailability, and therapeutic outcomes of various drugs, particularly in the context of targeted drug delivery and controlled release applications.
Check Digit Verification of cas no
The CAS Registry Mumber 165874-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,8,7 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 165874-29:
(8*1)+(7*6)+(6*5)+(5*8)+(4*7)+(3*4)+(2*2)+(1*9)=173
173 % 10 = 3
So 165874-29-3 is a valid CAS Registry Number.
165874-29-3Relevant academic research and scientific papers
Syntheses of the Fungicide/Insecticide Allosamidin and a Structural Isomer
Blattner, Regine,Furneaux, Richard H.,Kemmitt, timothy,Tyler, Peter C.,Ferrier, Robert J.,Tiden, Anna-Karin
, p. 3411 - 3422 (2007/10/02)
A synthesis of the naturally occurring inhibitor of chitin metabolism, allosamidin 1, involves, as the key step, condensation between the allosamizoline derivative 39, prepared following oxyamination of the cyclopentene 19, and the disaccharide glycosylating agent 54 which was synthesised from 2-acetamido-2-deoxy-D-glucose.The structural isomer 59 of allosamidin is also reported.Brief biological test results obtained using isomers 1 and 59 are recorded.
