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The chemical compound "(3aR,4R,5R,6aS)-4-[(E)-(R)-4-(4-Methoxy-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-2-ol core, which is a type of heterocyclic compound. The molecule is characterized by its hexahydro (six hydrogen atoms attached to a carbon chain) and tetrahydro-pyran-2-yloxy (a cyclic ether group) moieties, which contribute to its stability and reactivity. The compound also includes a but-1-enyl group with a double bond (E) and a chiral center (R), indicating that it has a specific three-dimensional arrangement of atoms. Additionally, it has a 4-methoxy-phenoxy group, which is a phenol derivative with a methoxy substituent, adding to its complexity. (3aR,4R,5R,6aS)-4-[(E)-(R)-4-(4-Methoxy-phenoxy)-3-(tetrahydro-pyran-2-yloxy)-but-1-enyl]-5-(tetrahydro-pyran-2-yloxy)-hexahydro-cyclopenta[b]furan-2-ol is likely to be found in the realm of pharmaceuticals or as an intermediate in organic synthesis due to its intricate structure and potential for specific interactions with biological targets.

79124-56-4

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79124-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79124-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,2 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79124-56:
(7*7)+(6*9)+(5*1)+(4*2)+(3*4)+(2*5)+(1*6)=144
144 % 10 = 4
So 79124-56-4 is a valid CAS Registry Number.

79124-56-4Downstream Products

79124-56-4Relevant 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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