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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)-

Benzenamine, 3-methoxy-4-methyl-

COc1cc(N)ccc1C Request for Quotation
Chemical Name: Benzenamine, 3-methoxy-4-methyl-
CAS Number: 16452-01-0
Product Number: AG007VFF(AGN-PC-0JKJPX)
Synonyms:
MDL No:
Molecular Formula: C8H11NO
Molecular Weight: 137.1790

Identification/Properties

Computed Properties
Molecular Weight:
137.182g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
137.084g/mol
Monoisotopic Mass:
137.084g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
10
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

PNMR/3-methoxy-4-methylaniline-16452-01-0-hnmr.pdf

Other Analytical Data

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Chemical Structure


The unique properties of 3-Methoxy-4-methylaniline make it a versatile compound in chemical synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its methoxy and methyl groups enhance the reactivity and selectivity of reactions, allowing for the precise manipulation of molecular structures. In organic synthesis, 3-Methoxy-4-methylaniline can be used as a key intermediate in the production of complex molecules, enabling the introduction of functional groups at specific positions. Additionally, its presence in the synthesis of dyes and pigments contributes to the vibrant colors and properties of these compounds. Overall, the strategic incorporation of 3-Methoxy-4-methylaniline in chemical reactions facilitates the efficient synthesis of diverse compounds with tailored functionalities and applications.