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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)-

Benzamide, 4-amino-

Nc1ccc(cc1)C(=O)N Request for Quotation
Chemical Name: Benzamide, 4-amino-
CAS Number: 2835-68-9
Product Number: AG003KQS(AGN-PC-0JLPS3)
Synonyms:
MDL No:
Molecular Formula: C7H8N2O
Molecular Weight: 136.1512

Identification/Properties

Properties
MP:
181-183 °C(lit.)
BP:
349°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.5769 (estimate)
Computed Properties
Molecular Weight:
136.154g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
136.064g/mol
Monoisotopic Mass:
136.064g/mol
Topological Polar Surface Area:
69.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
128
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Aminobenzamide, also known as 4-ABA, is a versatile compound widely used in chemical synthesis for its unique properties and wide range of applications. In organic chemistry, 4-aminobenzamide serves as a key intermediate in the synthesis of various compounds, including pharmaceuticals, dyes, and polymers. Its functional groups allow for diverse synthetic pathways, making it a valuable building block in the production of complex molecules. Additionally, 4-aminobenzamide is employed in biochemical research as a reagent for the detection and quantification of specific enzymes and proteins. Its ability to form stable complexes with certain biomolecules makes it a valuable tool in biological studies and drug development efforts. The versatility and utility of 4-aminobenzamide make it an essential component in modern chemical synthesis and research endeavors.