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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-[(2-cyanophenyl)sulfonyl-methylamino]acetic acid

N#Cc1ccccc1S(=O)(=O)N(CC(=O)O)C Request for Quotation
Chemical Name: 2-[(2-cyanophenyl)sulfonyl-methylamino]acetic acid
CAS Number: 1000931-63-4
Product Number: AG019L4W(AGN-PC-052FMI)
Synonyms:
MDL No: MFCD09863308
Molecular Formula: C10H10N2O4S
Molecular Weight: 254.2624

Identification/Properties

Computed Properties
Molecular Weight:
254.26g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
254.036g/mol
Monoisotopic Mass:
254.036g/mol
Topological Polar Surface Area:
107A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
431
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-(N-Methyl2-cyanobenzenesulfonamido)acetic Acid is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. In organic synthesis, this compound serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its functional groups allow for selective modification and derivatization, making it a valuable tool in the creation of complex organic molecules. Additionally, the presence of the sulfonyl group enhances the compound's stability and reactivity, enabling efficient transformations in synthetic routes. This compound is especially useful in the development of new drug candidates and specialty chemicals, showcasing its importance in modern chemical synthesis strategies.