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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)-

Isothiazolidine, 2-(4-bromophenyl)-, 1,1-dioxide

Brc1ccc(cc1)N1CCCS1(=O)=O Request for Quotation
Chemical Name: Isothiazolidine, 2-(4-bromophenyl)-, 1,1-dioxide
CAS Number: 71703-16-7
Product Number: AG005QJV(AGN-PC-0NJCOT)
Synonyms:
MDL No: MFCD09933347
Molecular Formula: C9H10BrNO2S
Molecular Weight: 276.1502

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
276.148g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
274.962g/mol
Monoisotopic Mass:
274.962g/mol
Topological Polar Surface Area:
45.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
290
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound isothiazolidine, 2-(4-bromophenyl)-, 1,1-dioxide plays a vital role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable intermediate in the preparation of various organic compounds. This compound is particularly useful in the development of pharmaceuticals, agrochemicals, and advanced materials. Its presence in chemical synthesis processes enables the creation of diverse molecules with desired properties and functions. By incorporating isothiazolidine, 2-(4-bromophenyl)-, 1,1-dioxide into synthetic pathways, chemists can efficiently access novel structures and enhance the scope of organic synthesis.