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[R-(R,S)]-3-(3-cyclohexyl-3-hydroxypropyl)-2,5-dioxoimidazolidine-4-heptanoic acid, also known as the (3R,4S)-enantiomer of BW 245C, is a chiral compound with a unique structure that features a cyclohexyl group, a hydroxypropyl group, and an imidazolidine ring. [R-(R,S)]-3-(3-cyclohexyl-3-hydroxypropyl)-2,5-dioxoimidazolidine-4-heptanoic acid has a specific stereochemistry that may contribute to its potential applications and properties.

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72880-75-2 Usage

Uses

Unfortunately, the provided materials do not include specific applications or industries for [R-(R,S)]-3-(3-cyclohexyl-3-hydroxypropyl)-2,5-dioxoimidazolidine-4-heptanoic acid. However, given its chiral nature and unique structure, it is possible that [R-(R*,S*)]-3-(3-cyclohexyl-3-hydroxypropyl)-2,5-dioxoimidazolidine-4-heptanoic acid could be used in various fields such as pharmaceuticals, materials science, or as a chiral building block in the synthesis of other complex molecules. Further research and information would be required to determine its specific uses and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 72880-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,8 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72880-75:
(7*7)+(6*2)+(5*8)+(4*8)+(3*0)+(2*7)+(1*5)=152
152 % 10 = 2
So 72880-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H32N2O5/c22-16(14-8-4-3-5-9-14)12-13-21-15(18(25)20-19(21)26)10-6-1-2-7-11-17(23)24/h14-16,22H,1-13H2,(H,23,24)(H,20,25,26)/t15-,16+/m0/s1

72880-75-2Relevant academic research and scientific papers

Heterocyclic Prostaglandin Analogues. Part 3. The Relationship of Configuration to Biological Activity for Some Hydantoin Prostanglandin Analogues

Brockwell, Michael A.,Caldwell, A. Gordon,Whittaker, Norman,Begley, Michael J.

, p. 706 - 711 (2007/10/02)

The enantiomers of the two diastereomers of 5-(6-carboxyhexyl)-1-(3-cyclohexyl-3-hydroxypropyl)hydantoin have been synthesised.Potent inhibition of platelet aggregation in this series is associated with the configuration corresponding to that in the natural inhibitors, such as prostaglandins E1 and D2.

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