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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)-

2-Benzothiazolesulfonamide

NS(=O)(=O)c1nc2c(s1)cccc2 Request for Quotation
Chemical Name: 2-Benzothiazolesulfonamide
CAS Number: 433-17-0
Product Number: AG00DICW(AGN-PC-0JL85I)
Synonyms:
MDL No:
Molecular Formula: C7H6N2O2S2
Molecular Weight: 214.2647

Identification/Properties

Computed Properties
Molecular Weight:
214.257g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
213.987g/mol
Monoisotopic Mass:
213.987g/mol
Topological Polar Surface Area:
110A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
285
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


2-Benzothiazolesulfonamide is a versatile compound widely utilized in chemical synthesis as a key building block in the production of various organic molecules. This compound plays a crucial role in the pharmaceutical industry, where it is frequently employed as a precursor in the synthesis of bioactive compounds and pharmaceutical drugs.In chemical synthesis, 2-Benzothiazolesulfonamide serves as a valuable starting material for the production of sulfonamides, which are important functional groups found in numerous pharmaceuticals. Its unique structure and reactivity enable it to participate in a wide range of transformations, making it a valuable tool for organic chemists seeking to create complex molecular structures.Furthermore, 2-Benzothiazolesulfonamide can undergo various functionalization reactions, allowing for the introduction of different substituents to tailor the properties of the final compound. This versatility makes it a highly sought-after reagent in drug discovery and development, where the ability to fine-tune the chemical structure is essential for optimizing the desired biological activity.Overall, the application of 2-Benzothiazolesulfonamide in chemical synthesis highlights its significance as a key intermediate in the preparation of diverse compounds with potential pharmaceutical and scientific applications.