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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-(4-nitrobenzoyl)-

OC(=O)CNC(=O)c1ccc(cc1)[N+](=O)[O-] Request for Quotation
Chemical Name: Glycine, N-(4-nitrobenzoyl)-
CAS Number: 2645-07-0
Product Number: AG002T9U(AGN-PC-0JKDJ1)
Synonyms:
MDL No:
Molecular Formula: C9H8N2O5
Molecular Weight: 224.1702

Identification/Properties

Properties
MP:
131-133℃(lit.)
BP:
531.2°C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
224.172g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
224.043g/mol
Monoisotopic Mass:
224.043g/mol
Topological Polar Surface Area:
112A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
291
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Nitrobenzamido)acetic acid, also known as N-(4-nitrobenzoyl)glycine, is a versatile compound frequently utilized in chemical synthesis. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique molecular properties.In chemical synthesis, 2-(4-Nitrobenzamido)acetic acid acts as a key intermediate in the production of complex organic molecules. Its nitrobenzamido group provides a reactive site for further chemical modifications, allowing for the introduction of diverse functional groups and facilitating the synthesis of structurally diverse compounds.Furthermore, the carboxylic acid functionality in 2-(4-Nitrobenzamido)acetic acid enables it to participate in a wide range of organic reactions, including esterification, amidation, and decarboxylation. This versatility makes it an essential component in the construction of peptide analogs, heterocyclic compounds, and chiral molecules with potential biological activities.Overall, the application of 2-(4-Nitrobenzamido)acetic acid in chemical synthesis plays a crucial role in the development of novel molecules with diverse functionalities and applications in pharmaceutical, agricultural, and materials science industries.