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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)-

Urea, (3-aminophenyl)-

NC(=O)Nc1cccc(c1)N Request for Quotation
Chemical Name: Urea, (3-aminophenyl)-
CAS Number: 25711-72-2
Product Number: AG00I4WX(AGN-PC-0JLGIQ)
Synonyms:
MDL No: MFCD00035935
Molecular Formula: C7H9N3O
Molecular Weight: 151.1659

Identification/Properties

Properties
BP:
321.033°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
151.169g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H317-H319-H335
Precautionary Statements:
P261-P264-P271-P272-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(3-Aminophenyl)urea, also known as 3-Aminophenylurea, is a versatile compound widely used in chemical synthesis as a key building block. This compound plays a crucial role in various organic reactions, particularly in the development of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 1-(3-Aminophenyl)urea serves as a valuable intermediate for the preparation of diverse organic compounds due to its unique reactivity and structural properties. Its amino and urea functional groups make it a suitable candidate for the synthesis of heterocyclic compounds, biologically active molecules, and complex organic frameworks.One prominent application of 1-(3-Aminophenyl)urea is in the synthesis of urea derivatives with specific biological activities. By incorporating this compound into the molecular structure, chemists can modulate the physicochemical properties and pharmacological profile of the resulting compounds. Additionally, its presence can enhance the stability, solubility, and bioavailability of the final products.Furthermore, 1-(3-Aminophenyl)urea can be utilized in the preparation of polymeric materials with tailored properties. Its ability to participate in polymerization reactions allows for the creation of novel polymer architectures with desired functionalities, such as enhanced mechanical strength, thermal stability, and biocompatibility.Overall, the application of 1-(3-Aminophenyl)urea in chemical synthesis offers significant opportunities for designing and synthesizing diverse organic compounds with valuable properties for various industrial sectors. Its versatility and reactivity make it a valuable tool for chemists seeking to develop novel molecules with specific applications in pharmaceuticals, materials science, and beyond.