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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, phenyl-

NC(=O)Nc1ccccc1 Request for Quotation
Chemical Name: Urea, phenyl-
CAS Number: 64-10-8
Product Number: AG00E94N(AGN-PC-07229Q)
Synonyms:
MDL No:
Molecular Formula: C7H8N2O
Molecular Weight: 136.1512

Identification/Properties

Properties
MP:
145-147°C(lit.);
BP:
238.0°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5769 (estimate)
Solubility:
H2O: 10 mg/mL, clear
Computed Properties
Molecular Weight:
136.154g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
136.064g/mol
Monoisotopic Mass:
136.064g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
119
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Phenylurea, also known as phenylcarbamide, is a versatile chemical compound widely utilized in chemical synthesis processes. This organic compound plays a crucial role in various chemical reactions due to its unique properties and reactivity.In chemical synthesis, 1-Phenylurea serves as a key building block for the production of diverse compounds. It acts as a potent nucleophile in nucleophilic addition reactions, facilitating the formation of new carbon-carbon or carbon-nitrogen bonds. Additionally, 1-Phenylurea can undergo substitution reactions, enabling the introduction of different functional groups into organic molecules.Furthermore, 1-Phenylurea is frequently employed as a ligand in coordination chemistry, where it can form stable complexes with various metal ions. These complexes exhibit distinct properties and can be utilized in catalytic processes, such as asymmetric synthesis and metal-catalyzed reactions.Overall, the application of 1-Phenylurea in chemical synthesis is diverse and essential for the construction of complex organic molecules with specific functionalities. Its versatility and reactivity make it a valuable compound in the realm of synthetic chemistry.