Welcome to LookChem.com Sign In|Join Free
  • or
The chemical compound "(3aR,4R,5R,6aS)-5-(Tetrahydro-pyran-2-yloxy)-4-[(E)-(R)-3-(tetrahydro-pyran-2-yloxy)-4-m-tolyloxy-but-1-enyl]-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 contains multiple chiral centers, indicated by the (3aR,4R,5R,6aS) configuration, suggesting that it has specific three-dimensional arrangements of its atoms. It also has several tetrahydro-pyran-2-yloxy groups, which are ether moieties derived from tetrahydro-pyran, a cyclic structure. Additionally, the compound includes a but-1-enyl side chain with a double bond (E) and a 4-m-tolyloxy substituent, indicating the presence of a methyl group on the phenol ring. This intricate arrangement of functional groups and stereochemistry suggests that the compound may have specific biological activities or be used in the synthesis of other complex molecules.

79124-53-1

Post Buying Request

79124-53-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

79124-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79124-53-1 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 79124-53:
(7*7)+(6*9)+(5*1)+(4*2)+(3*4)+(2*5)+(1*3)=141
141 % 10 = 1
So 79124-53-1 is a valid CAS Registry Number.

79124-53-1Relevant 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).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 79124-53-1