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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-amino-2-methyl-

Nc1ccc(c(c1)C)O Request for Quotation
Chemical Name: Phenol, 4-amino-2-methyl-
CAS Number: 2835-96-3
Product Number: AG00I5BK(AGN-PC-0JLPS5)
Synonyms:
MDL No:
Molecular Formula: C7H9NO
Molecular Weight: 123.15246

Identification/Properties

Computed Properties
Molecular Weight:
123.155g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
123.068g/mol
Monoisotopic Mass:
123.068g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
94.9
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 4-Amino-2-methylphenol plays a crucial role as a versatile building block. This compound, also known as p-Aminocresol, is commonly utilized in the production of various organic compounds and materials. Its unique chemical properties make it a valuable intermediate in the synthesis of dyes, pharmaceuticals, and other specialty chemicals.One of the key applications of 4-Amino-2-methylphenol is its use in the synthesis of azo dyes. By reacting with diazonium salts derived from aromatic amines, this compound can be incorporated into the dye molecule, contributing to its color and functionality. The presence of the amino group and the methyl substituent on the phenol ring enables precise control over the dye's properties, such as solubility, stability, and hue.Additionally, 4-Amino-2-methylphenol is employed in the pharmaceutical industry for the synthesis of certain drug molecules. Its structural features make it an important building block for pharmaceutical intermediates and active pharmaceutical ingredients (APIs). By selectively modifying the amine or phenol groups, chemists can tailor the molecular structure of the final drug compound to enhance its biological activity and pharmacokinetic properties.Furthermore, in organic synthesis, this compound can participate in various reactions such as acylation, alkylation, and oxidation to introduce functional groups or modify its chemical structure. Its versatility and reactivity make it a valuable tool for the preparation of diverse organic molecules with specific properties and applications in fields ranging from materials science to agrochemicals.Overall, 4-Amino-2-methylphenol's significance in chemical synthesis lies in its ability to serve as a fundamental building block for the creation of complex and functional organic molecules, contributing to advancements in various industries and scientific research areas.