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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)-

Ethanesulfonic acid, 2-(methylamino)-

CNCCS(=O)(=O)O Request for Quotation
Chemical Name: Ethanesulfonic acid, 2-(methylamino)-
CAS Number: 107-68-6
Product Number: AG003807(AGN-PC-0JK8AK)
Synonyms:
MDL No:
Molecular Formula: C3H9NO3S
Molecular Weight: 139.1735

Identification/Properties

Computed Properties
Molecular Weight:
139.169g/mol
XLogP3:
-3.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
139.03g/mol
Monoisotopic Mass:
139.03g/mol
Topological Polar Surface Area:
74.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
133
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


N-Methyltaurine, also known as 2-Aminoethanesulfonic Acid N-Methyl Derivative, plays a vital role in chemical synthesis as a versatile building block and reagent. With its unique structure and properties, N-Methyltaurine is extensively used in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its incorporation in chemical synthesis processes enables the efficient formation of complex molecules and scaffolds, making it a valuable resource for medicinal and material chemistry research. This compound's reactivity and compatibility with a wide range of reaction conditions further enhance its applicability in the development of novel organic compounds with diverse functionalities.