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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-aminobenzoyl)-, monosodium salt

NC(C(=O)[O-])NC(=O)c1ccccc1.[Na+] Request for Quotation
Chemical Name: Glycine, N-(4-aminobenzoyl)-, monosodium salt
CAS Number: 94-16-6
Product Number: AG003UB9(AGN-PC-0W3TFU)
Synonyms:
MDL No:
Molecular Formula: C9H9N2NaO3
Molecular Weight: 216.1691

Identification/Properties

Properties
MP:
123-125°C
BP:
517.2°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
216.172g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
216.051g/mol
Monoisotopic Mass:
216.051g/mol
Topological Polar Surface Area:
95.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
227
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Aminohippurate sodium, also known as Sodium para-aminohippurate, is a key compound commonly used in chemical synthesis processes within the field of pharmaceuticals and organic chemistry. Its primary application lies in the determination of renal plasma flow in medical diagnostics. This compound plays a crucial role in aiding the measurement of effective renal plasma flow through the use of clearance methods, making it a valuable tool in assessing kidney function. Furthermore, Aminohippurate sodium exhibits unique properties that make it a versatile reagent for various organic transformations, including esterifications and amidations, thereby enabling its utility in the synthesis of pharmaceutical intermediates and complex organic molecules. Its compatibility with a wide range of reaction conditions and the ability to selectively target specific functional groups make it a desirable component in chemical reactions requiring precise control and efficiency.