855609-52-8 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 14 carbon (C) atoms, 11 hydrogen (H) atoms, 1 chlorine (Cl) atom, 1 oxygen (O) atom, and 1 sulfur (S) atom.
Explanation
The compound is derived from thiophene, which is a five-membered aromatic ring containing sulfur. It has a 3-chlorophenyl group (a phenyl group with a chlorine atom at the 3rd position) attached to the 5th position of the thiophene ring. Additionally, an ethanone group (a carbonyl group attached to two carbon atoms, forming a two-carbon chain) is attached to the thiophene ring.
Explanation
The compound has three main functional groups the thiophene ring, which is a heterocyclic aromatic ring containing sulfur; the 3-chlorophenyl group, which is a phenyl group with a chlorine atom substitution; and the ethanone group, which is a carbonyl group attached to a two-carbon chain.
Explanation
Due to its unique structure and potential biological activity, 1-[5-(3-chlorophenyl)thiophene-2-yl]ethanone is commonly used in organic synthesis and pharmaceutical research. It may be used in the development of new drugs or as a building block for other organic compounds.
Explanation
The compound's unique structure and functional groups may provide it with specific biological activities that could be useful in the development of new drugs or therapies.
Explanation
The presence of aromatic rings (thiophene and phenyl) in the compound contributes to its stability. The delocalized π-electrons in these rings provide increased stability and resistance to reactions that would disrupt the aromaticity.
Explanation
The compound's functional groups, such as the thiophene ring, 3-chlorophenyl group, and ethanone group, can participate in various chemical reactions, such as electrophilic aromatic substitution, nucleophilic addition, and carbonyl group reactions.
Structure
Thiophene derivative with a 3-chlorophenyl group at the 5-position and an ethanone group attached to the thiophene ring.
Aromaticity
Contains an aromatic thiophene ring and a phenyl ring.
Functional groups
Thiophene ring, 3-chlorophenyl group, and ethanone group.
Applications
Organic synthesis and pharmaceutical research.
Potential biological activity
May have applications in the development of new drugs.
Stability
Relatively stable due to its aromatic rings and delocalized π-electrons.
Reactivity
May undergo various reactions due to the presence of functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 855609-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,6,0 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 855609-52:
(8*8)+(7*5)+(6*5)+(5*6)+(4*0)+(3*9)+(2*5)+(1*2)=198
198 % 10 = 8
So 855609-52-8 is a valid CAS Registry Number.
855609-52-8Relevant articles and documents
Synthesis of functionalized 2-arylthiophenes with triarylbismuths as atom-efficient multicoupling organometallic nucleophiles under palladium catalysis
Rao, Maddali L. N.,Banerjee, Debasis,Dhanorkar, Ritesh J.
supporting information; experimental part, p. 1324 - 1330 (2011/07/07)
Atom-efficient cross-coupling reactions of functionalized 2-bromo- and 2-iodothiophenes have been demonstrated using triarylbismuths as atom-efficient multicoupling organometallic nucleophiles under palladium-catalyzed conditions. These couplings with various functionalized triarylbismuths proceeded smoothly to afford the corresponding functionalized 2-arylthiophenes in high yields. Georg Thieme Verlag Stuttgart · New York.
