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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-bromo-N-methyl-

CNc1cccc(c1)Br Request for Quotation
Chemical Name: Benzenamine, 3-bromo-N-methyl-
CAS Number: 66584-32-5
Product Number: AG00FE9B(AGN-PC-0LW82P)
Synonyms:
MDL No:
Molecular Formula: C7H8BrN
Molecular Weight: 186.0491

Identification/Properties

Properties
BP:
253°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.6120(lit.)
Computed Properties
Molecular Weight:
186.052g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
184.984g/mol
Monoisotopic Mass:
184.984g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
85
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Bromo-N-methylaniline, also known as 3-Bromo-1-methylaniline, is a versatile chemical compound widely used in chemical synthesis. This compound plays a key role as a building block in the creation of various organic molecules due to its unique properties and reactivity. One of the primary applications of 3-Bromo-N-methylaniline in chemical synthesis is in the pharmaceutical industry. It is utilized as a key intermediate in the synthesis of various pharmaceutical compounds, including antiviral drugs, antibiotics, and anti-cancer medications. The bromine atom on the aromatic ring of 3-Bromo-N-methylaniline can serve as a convenient handle for further functionalization, allowing for the introduction of specific chemical groups necessary for enhancing the biological activity of the final drug molecule.Additionally, 3-Bromo-N-methylaniline is a valuable building block in the production of dyes and pigments. Its aromatic structure and bromine substituent make it an ideal precursor in the synthesis of colored organic compounds used in the textile and printing industries. By selectively modifying the bromine position or introducing other functional groups, chemists can tailor the properties of the resulting dyes for specific applications, such as improving color fastness or light stability.Furthermore, 3-Bromo-N-methylaniline is employed in the synthesis of various agrochemicals and specialty chemicals. Its versatile reactivity allows for the creation of complex molecular structures required for herbicides, insecticides, and other agricultural products. By strategically incorporating 3-Bromo-N-methylaniline into the chemical synthesis route, chemists can efficiently access a wide range of functionalized compounds with diverse applications in the agricultural sector.In conclusion, 3-Bromo-N-methylaniline serves as a valuable building block in chemical synthesis, particularly in the pharmaceutical, dye, pigment, and agrochemical industries. Its reactivity and structural features make it a versatile precursor for the creation of a wide variety of organic molecules with tailored properties for specific applications.