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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzenesulfonylchloride, 5-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-2-methoxy-

COc1ccc(cc1S(=O)(=O)Cl)N1C(=O)c2c(C1=O)cccc2 Request for Quotation
Chemical Name: Benzenesulfonylchloride, 5-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-2-methoxy-
CAS Number: 885279-82-3
Product Number: AG0089A2(AGN-PC-001KVG)
Synonyms:
MDL No:
Molecular Formula: C15H10ClNO5S
Molecular Weight: 351.7616

Identification/Properties

Computed Properties
Molecular Weight:
351.757g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
350.997g/mol
Monoisotopic Mass:
350.997g/mol
Topological Polar Surface Area:
89.1A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
578
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

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 5-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)-2-methoxybenzenesulfonyl chloride is a versatile chemical compound commonly employed in chemical synthesis processes. This compound serves as a key reagent in the preparation of various organic molecules due to its unique structural features and reactivity.One of the primary applications of 5-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)-2-methoxybenzenesulfonyl chloride is as a sulfonylating agent in organic synthesis. It participates in sulfonation reactions, where it introduces a sulfonyl group onto target molecules, leading to the formation of new compounds with modified properties. This functional group can impart enhanced stability, solubility, or reactivity to the final products, making it crucial in the development of advanced materials and pharmaceutical substances.Furthermore, this sulfonyl chloride derivative is utilized in the construction of complex molecular architectures through its ability to selectively react with specific functional groups in the presence of other reactive moieties. It can act as a key building block in multi-step synthesis routes, enabling the efficient assembly of intricate chemical structures with high precision and selectivity.Overall, the 5-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)-2-methoxybenzenesulfonyl chloride plays a significant role in the realm of chemical synthesis by facilitating the creation of novel organic compounds and enabling the exploration of diverse chemical pathways for the development of advanced materials and pharmaceuticals.