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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)-

Phenol, 3-(phenylamino)-

Oc1cccc(c1)Nc1ccccc1 Request for Quotation
Chemical Name: Phenol, 3-(phenylamino)-
CAS Number: 101-18-8
Product Number: AG0003FP(AGN-PC-0JK84U)
Synonyms:
MDL No:
Molecular Formula: C12H11NO
Molecular Weight: 185.2218

Identification/Properties

Properties
MP:
81-82 °C
BP:
340.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
1.5300 (estimate)
Computed Properties
Molecular Weight:
185.226g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
185.084g/mol
Monoisotopic Mass:
185.084g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
166
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#:
N/A
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Phenylamino)phenol, also known as Catecholamine, is a versatile compound often utilized in chemical synthesis for its unique properties. In the field of organic chemistry, this compound serves as a valuable building block in the synthesis of various complex molecules. Thanks to its aromatic structure and functional groups, 3-(Phenylamino)phenol can participate in a wide range of reactions, enabling the formation of new bonds and structures.One notable application of 3-(Phenylamino)phenol is in the synthesis of dyes and pigments. Its benzene ring, combined with the amino and hydroxyl groups, allows for the creation of vivid and stable colorants for various industries, such as textiles, paints, and plastics. Additionally, this compound can be employed in the production of pharmaceuticals, where its functional groups can be modified to introduce specific properties or enhance biological activity.In the realm of materials science, 3-(Phenylamino)phenol plays a crucial role in the development of polymers and coatings. By incorporating this compound into polymer chains, researchers can tailor the physical and chemical properties of the material, leading to improved performance and durability. Moreover, the presence of the phenylamino group can facilitate adhesion to substrates, making it a valuable component in adhesives and sealants.Overall, 3-(Phenylamino)phenol stands as a valuable tool in chemical synthesis, offering diverse possibilities for creating novel compounds with desirable properties. Its versatility and reactivity make it a sought-after ingredient in various industries, where its applications span from dyes and pharmaceuticals to materials and beyond.