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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)-

Benzoic acid, 3-amino-, hydrazide

NNC(=O)c1cccc(c1)N Request for Quotation
Chemical Name: Benzoic acid, 3-amino-, hydrazide
CAS Number: 14062-34-1
Product Number: AG001CL9(AGN-PC-0JLUXU)
Synonyms:
MDL No:
Molecular Formula: C7H9N3O
Molecular Weight: 151.1659

Identification/Properties

Properties
MP:
91-92°C
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
151.169g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
151.075g/mol
Monoisotopic Mass:
151.075g/mol
Topological Polar Surface Area:
81.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Aminobenzohydrazide is a key chemical compound widely used in chemical synthesis applications. With its unique structure and properties, this versatile molecule serves as a valuable building block in the synthesis of various organic compounds. In the field of medicinal chemistry, 3-Aminobenzohydrazide plays a crucial role in the development of pharmaceuticals and drug design. Its reactivity allows for the creation of diverse derivatives that exhibit potential biological activities, making it an essential component in the discovery of new therapeutic agents. Furthermore, this compound is utilized in the preparation of heterocyclic compounds, dyes, and agrochemicals, showcasing its significance across different industries. In organic synthesis, 3-Aminobenzohydrazide serves as a fundamental precursor for the formation of hydrazones, oximes, and other functional groups, enabling chemists to access a wide range of chemical transformations. Its ability to participate in various reactions makes it a valuable tool for designing complex molecular structures and advancing synthetic methods. In summary, the application of 3-Aminobenzohydrazide in chemical synthesis spans across multiple disciplines, highlighting its importance in the creation of novel compounds and materials.