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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)-

2-(Aminomethyl)-6-methylphenol hydrochloride

NCc1cccc(c1O)C.Cl Request for Quotation
Chemical Name: 2-(Aminomethyl)-6-methylphenol hydrochloride
CAS Number: 1956330-87-2
Product Number: AG00I3FV(AGN-PC-0WAMIS)
Synonyms:
MDL No:
Molecular Formula: C8H12ClNO
Molecular Weight: 173.6400

Identification/Properties

Computed Properties
Molecular Weight:
173.64g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
173.061g/mol
Monoisotopic Mass:
173.061g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
105
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Aminomethyl)-6-methylphenol hydrochloride is a versatile compound commonly used in chemical synthesis applications. This compound plays a crucial role in organic chemistry, particularly in the synthesis of various pharmaceuticals and fine chemicals. Its unique chemical properties make it an essential building block for the creation of a wide range of complex molecules.One of the key applications of 2-(Aminomethyl)-6-methylphenol hydrochloride in chemical synthesis is its involvement in the preparation of heterocyclic compounds. By serving as a starting material or intermediate in chemical reactions, this compound contributes to the formation of diverse heterocycles, which are vital in drug discovery and material science. The hydrochloride form of this compound enhances its solubility and facilitates its use in various aqueous reactions.Moreover, 2-(Aminomethyl)-6-methylphenol hydrochloride is commonly employed as a reagent in organic transformations, such as Mannich reactions and condensation reactions. These reactions enable the introduction of the aminomethyl group into target molecules, allowing chemists to modify and functionalize organic compounds for specific purposes. The compound's ability to participate in these reactions with high selectivity and efficiency makes it a valuable tool in synthetic chemistry.In summary, 2-(Aminomethyl)-6-methylphenol hydrochloride is a crucial component in chemical synthesis, offering a broad range of applications in the creation of various organic compounds. Its versatility, reactivity, and solubility in aqueous environments make it an indispensable reagent for the synthesis of pharmaceuticals, heterocyclic compounds, and other fine chemicals.