107137-02-0 Usage
Molecular structure
The compound has a complex molecular structure that includes a phenanthro-furan core, multiple rings, and side chains. The presence of these structural elements contributes to its unique chemical properties and reactivity.
Acetate derivative
This compound is an acetate derivative, which means it has an ester functional group (-COO-) attached to the furan ring. This feature can affect its solubility, reactivity, and compatibility with other chemicals.
Stereochemistry
The compound has specific stereochemistry, indicated by the (3aR,5aS,10bS,10cR) notation. This means that the molecule has a particular 3D arrangement of its atoms, which can significantly impact its physical and chemical properties, as well as its potential applications.
Multiple substituents
The compound contains various substituents, such as methyl and isopropyl groups, which contribute to its complexity and diversity. These groups can influence the compound's polarity, solubility, and reactivity with other chemicals.
Potential applications
Due to its complex structure and unique properties, this compound may have various applications in organic synthesis, pharmaceuticals, and other industrial processes. Its reactivity and compatibility with other chemicals can make it a valuable building block or intermediate in the synthesis of more complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 107137-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,3 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 107137-02:
(8*1)+(7*0)+(6*7)+(5*1)+(4*3)+(3*7)+(2*0)+(1*2)=90
90 % 10 = 0
So 107137-02-0 is a valid CAS Registry Number.
107137-02-0Relevant articles and documents
The synthesis and antibacterial activity of totarol derivatives. Part 3: modification of ring-B
Evans, Gary B.,Furneaux, Richard H.,Gainsford, Graeme J.,Murphy, Michael P.
, p. 1663 - 1675 (2007/10/03)
Ring-B derivatization of totarol (1) afforded the series of compounds 2-22 which were screened in vitro against: β-lactamase-positive and high level gentamycin-resistant Enterococcus faecalis, penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus (MRSA), and multiresistant Klebsiella pneumoniae. Several of the derivatives retained much of the antibacterial activity of totatol against the first three of these organisms (all Gram-positive), but none was more active. The Gram-negative Klebsiella was resistant to all compounds examined. Totarol (1) was shown to uncouple oxidative phosphorylation in isolated mitochondria at 50 μM. Copyright (C) 2000 Elsevier Science Ltd.
