1H-Indene-5-sulfonyl chloride, 2,3-dihydro-1-oxo-


Chemical Name: 1H-Indene-5-sulfonyl chloride, 2,3-dihydro-1-oxo-
CAS Number: 61565-36-4
Product Number: AG019LI3(AGN-PC-002N73)
Synonyms:
MDL No:
Molecular Formula: C9H7ClO3S
Molecular Weight: 230.6681

Identification/Properties


Computed Properties
Molecular Weight:
230.662g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
229.98g/mol
Monoisotopic Mass:
229.98g/mol
Topological Polar Surface Area:
59.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
344
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



1-Oxo-2,3-dihydro-1H-indene-5-sulfonyl chloride, also known as $name$, is a versatile compound used in chemical synthesis for various important reactions. This compound serves as an effective sulfonylating agent in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and functional materials.$name$ is commonly employed in the introduction of sulfonyl groups into organic molecules, allowing for the modification of their chemical properties. This compound is utilized in the formation of carbon-sulfur bonds, which are valuable for creating new chemical entities with diverse functionalities.In addition, $name$ plays a key role in the synthesis of complex organic compounds by enabling the selective introduction of sulfonyl moieties at specific positions within a molecule. Its reactivity and selectivity make it a valuable tool for chemists working on the design and development of novel compounds for various applications.Furthermore, $name$ can act as a protective group in organic synthesis, where it temporarily shields specific functional groups in a molecule from unwanted reactions, allowing for selective transformations to occur at other sites. This protective strategy is crucial in multi-step synthesis processes to achieve desired products efficiently.Overall, the application of 1-Oxo-2,3-dihydro-1H-indene-5-sulfonyl chloride in chemical synthesis provides chemists with a powerful tool for modifying, functionalizing, and protecting organic molecules, thereby facilitating the development of new materials and bioactive compounds.