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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)-

7-Benzofuransulfonylchloride, 5-bromo-2,3-dihydro-

Brc1cc2CCOc2c(c1)S(=O)(=O)Cl Request for Quotation
Chemical Name: 7-Benzofuransulfonylchloride, 5-bromo-2,3-dihydro-
CAS Number: 690632-00-9
Product Number: AG005LRY(AGN-PC-0KL74C)
Synonyms:
MDL No:
Molecular Formula: C8H6BrClO3S
Molecular Weight: 297.5534

Identification/Properties

Properties
Form:
Solid
Computed Properties
Molecular Weight:
297.547g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
295.891g/mol
Monoisotopic Mass:
295.891g/mol
Topological Polar Surface Area:
51.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
313
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-Bromo-2,3-dihydrobenzofuran-7-sulfonyl chloride is a versatile compound used in chemical synthesis for various applications. It serves as a key building block in the synthesis of complex organic molecules due to its reactivity and functional groups. Specifically, this compound is utilized in the preparation of sulfonamide derivatives, pharmaceutical intermediates, and agrochemicals. Its unique structure enables it to participate in a range of chemical reactions, such as nucleophilic substitution, coupling reactions, and cyclization reactions, making it an invaluable tool in organic synthesis. This compound plays a crucial role in the development of new drugs, materials, and specialty chemicals, showcasing its significance in modern chemistry research and development.