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The chemical compound "(3aR,4R,5R,6aS)-4-[(E)-(R)-4-(4-Fluoro-phenoxy)-3-(tetrahydro-pyran-2-yloxy)-but-1-enyl]-5-(tetrahydro-pyran-2-yloxy)-hexahydro-cyclopenta[b]furan-2-ol" is a complex organic molecule with a unique structure. It features a cyclopenta[b]furan core, which is a five-membered ring fused to a furan ring. The molecule has a hexahydro structure, indicating the presence of six hydrogen atoms bonded to carbon in a cyclic manner. It also contains two tetrahydro-pyran-2-yloxy groups, which are ether functional groups derived from tetrahydro-2-pyranol. One of the substituents on the but-1-enyl chain is a 4-fluoro-phenoxy group, providing a fluorine atom attached to a phenyl ring. The compound's stereochemistry is defined by the (3aR,4R,5R,6aS) configuration, which specifies the three-dimensional arrangement of atoms around the asymmetric centers. This complex structure likely confers specific biological or chemical properties, although the exact applications or functions are not specified in the provided information.

55444-98-9

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55444-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55444-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,4 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55444-98:
(7*5)+(6*5)+(5*4)+(4*4)+(3*4)+(2*9)+(1*8)=139
139 % 10 = 9
So 55444-98-9 is a valid CAS Registry Number.

55444-98-9Relevant academic research and scientific papers

N-(Methanesulfonyl)-16-phenoxyprostaglandincarboxamides: Tissue-Selective, Uterine Stimulants

Schaaf, Thomas K.,Bindra, Jasjit S.,Eggler, James F.,Plattner, Jacob J.,Nelson, A. James,et al.

, p. 1353 - 1359 (2007/10/02)

In an effort to develop tissue-selective prostaglandin analogues resistant to the metabolic inactivating pathways of the natural materials, hybrid compounds modified both at C-1 with a sulfonimide moiety and in the n-amylcarbinol side chain with substituted phenoxy groups were synthesized and evaluated in a variety of in vitro and in vivo models.Several of these analogues exhibited potent, tissue-selective, uterine stimulant activity, a finding subsequently confirmed in clinical studies with one member of this series, N-(methanesulfonyl)-16-phenoxy-ω-tetranor-PGE2-carboxamide (CP-34089/ZK-57671, sulprostone).

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