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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)-

Glycine, N-[[5-(dimethylamino)-1-naphthalenyl]sulfonyl]-N-methyl-

OC(=O)CN(S(=O)(=O)c1cccc2c1cccc2N(C)C)C Request for Quotation
Chemical Name: Glycine, N-[[5-(dimethylamino)-1-naphthalenyl]sulfonyl]-N-methyl-
CAS Number: 1093-96-5
Product Number: AG003ARJ(AGN-PC-0JLNUU)
Synonyms:
MDL No:
Molecular Formula: C15H18N2O4S
Molecular Weight: 322.3794

Identification/Properties

Computed Properties
Molecular Weight:
322.379g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
322.099g/mol
Monoisotopic Mass:
322.099g/mol
Topological Polar Surface Area:
86.3A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
500
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-[[5-(Dimethylamino)-1-naphthalenyl]sulfonyl]-N-methylglycine is a versatile compound widely used in chemical synthesis as a key reagent for the preparation of various functionalized molecules. It serves as a crucial building block in the synthesis of pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.In organic synthesis, N-[[5-(Dimethylamino)-1-naphthalenyl]sulfonyl]-N-methylglycine is commonly employed as a protecting group for amines, allowing for selective reactions at other functional groups while keeping the amine moiety inert. This feature is particularly valuable in complex multi-step syntheses where precise control over the reaction pathway is essential.Furthermore, this compound is a valuable tool in peptide chemistry, enabling the preparation of peptide derivatives with enhanced stability and selectivity. By incorporating N-[[5-(Dimethylamino)-1-naphthalenyl]sulfonyl]-N-methylglycine into peptide synthesis strategies, chemists can achieve better control over peptide bond formation and side chain protection, leading to improved yields and purities of the final products.Overall, the application of N-[[5-(Dimethylamino)-1-naphthalenyl]sulfonyl]-N-methylglycine in chemical synthesis plays a crucial role in expanding the toolkit available to synthetic chemists, ultimately facilitating the efficient and selective construction of complex molecules with diverse functionalities.