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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)-

1H-1-Benzazepine-7-sulfonyl chloride, 2,3,4,5-tetrahydro-2-oxo-

O=C1CCCc2c(N1)ccc(c2)S(=O)(=O)Cl Request for Quotation
Chemical Name: 1H-1-Benzazepine-7-sulfonyl chloride, 2,3,4,5-tetrahydro-2-oxo-
CAS Number: 927869-56-5
Product Number: AG006DXS(AGN-PC-00SXJG)
Synonyms:
MDL No: MFCD11099485
Molecular Formula: C10H10ClNO3S
Molecular Weight: 259.7093

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;
Computed Properties
Molecular Weight:
259.704g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
259.007g/mol
Monoisotopic Mass:
259.007g/mol
Topological Polar Surface Area:
71.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
376
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepine-7-sulfonyl chloride is a versatile compound commonly used in chemical synthesis for its ability to act as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it an essential reagent in the production of a wide range of bioactive molecules and functional materials. In particular, this compound is often employed in the synthesis of sulfonamide-based drugs, as well as in the development of new chemical entities with potential therapeutic applications. Its sulfonamide functionality allows for facile modification and derivatization, enabling chemists to tailor molecular structures for specific purposes. In addition, the sulfonamide group can participate in a variety of chemical transformations, making this compound a valuable tool for the design and synthesis of complex organic molecules.