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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)-

Methanesulfonamide, N-(2-formylphenyl)-

O=Cc1ccccc1NS(=O)(=O)C Request for Quotation
Chemical Name: Methanesulfonamide, N-(2-formylphenyl)-
CAS Number: 94532-99-7
Product Number: AG003F31(AGN-PC-00BZI5)
Synonyms:
MDL No: MFCD11052341
Molecular Formula: C8H9NO3S
Molecular Weight: 199.2270

Identification/Properties

Properties
BP:
350.192°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
199.224g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
199.03g/mol
Monoisotopic Mass:
199.03g/mol
Topological Polar Surface Area:
71.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
268
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Methylsulfonamido)benzaldehyde, a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. This compound acts as a key intermediate in the production of various pharmaceuticals, agrochemicals, and organic compounds. Its ability to undergo various reactions such as condensation, oxidation, and reduction makes it an essential building block in organic chemistry. In addition, its sulfonamido group provides a strategic site for further functionalization, enabling the synthesis of complex molecules with specific properties. Furthermore, 2-(Methylsulfonamido)benzaldehyde plays a crucial role in the development of new materials, catalysts, and fine chemicals, showcasing its significance in modern synthetic chemistry.