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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, 4-(2-naphthalenylamino)-

Oc1ccc(cc1)Nc1ccc2c(c1)cccc2 Request for Quotation
Chemical Name: Phenol, 4-(2-naphthalenylamino)-
CAS Number: 93-45-8
Product Number: AG00IHFW(AGN-PC-0JK7XS)
Synonyms:
MDL No:
Molecular Formula: C16H13NO
Molecular Weight: 235.2805

Identification/Properties

Properties
BP:
424.4°C at 760 mmHg
Computed Properties
Molecular Weight:
235.286g/mol
XLogP3:
4.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
235.1g/mol
Monoisotopic Mass:
235.1g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
260
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:
H302-H315-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Naphthalen-2-ylamino)phenol, sometimes referred to as Naphtholamine, is a versatile compound commonly used in chemical synthesis. Its unique structure and properties make it a valuable reagent in various reactions and processes across different areas of chemistry.One notable application of 4-(Naphthalen-2-ylamino)phenol is in the synthesis of dyes and pigments. As a key building block in the production of organic dyes, this compound plays a crucial role in determining the color and properties of the final product. Its aromatic ring system and amino group allow for selective functionalization, enabling the creation of a wide range of vibrant and stable dyes used in textiles, inks, and other industries.In addition to its significance in dye chemistry, 4-(Naphthalen-2-ylamino)phenol is also utilized in the synthesis of pharmaceuticals and agrochemicals. Its ability to participate in various coupling reactions and functional group transformations makes it a valuable intermediate in the preparation of biologically active compounds. By incorporating this compound into molecular structures, chemists can tailor the properties and efficacy of pharmaceuticals and crop protection agents, contributing to advancements in healthcare and agriculture.Furthermore, 4-(Naphthalen-2-ylamino)phenol has found its place in the realm of material science, where it serves as a building block for the synthesis of polymers and advanced materials. Through controlled polymerization and modification processes, scientists can harness the properties of this compound to design innovative materials with specific characteristics such as conductivity, optical properties, or mechanical strength. These materials find applications in electronic devices, coatings, and other high-tech industries, driving progress in diverse fields of technology.Overall, the versatile nature of 4-(Naphthalen-2-ylamino)phenol makes it a valuable tool in chemical synthesis, offering unique opportunities for chemists to create a wide array of functional molecules with applications ranging from dyes and pharmaceuticals to advanced materials.