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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, 2-chloro-N-methyl-

CNc1ccccc1Cl Request for Quotation
Chemical Name: Benzenamine, 2-chloro-N-methyl-
CAS Number: 932-32-1
Product Number: AG006HNJ(AGN-PC-0JMP21)
Synonyms:
MDL No:
Molecular Formula: C7H8ClN
Molecular Weight: 141.5981

Identification/Properties

Properties
BP:
218 °C(lit.)
Storage:
Light sensitive;Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.579(lit.)
Solubility:
Not miscible or difficult to mix.
Computed Properties
Molecular Weight:
141.598g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
141.035g/mol
Monoisotopic Mass:
141.035g/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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-N-methylaniline, a chemical compound with the molecular formula C7H8ClN, plays a crucial role in chemical synthesis processes. It is commonly utilized as a building block in the creation of various organic compounds due to its unique chemical properties. One significant application of 2-Chloro-N-methylaniline is its use as a key intermediate in the production of dyes and pigments. By undergoing further chemical reactions, this compound can be transformed into various colored molecules that are vital in the textile and printing industries. Additionally, it serves as a precursor for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.Furthermore, 2-Chloro-N-methylaniline is frequently employed in the preparation of organic compounds with biological activity. Its structure allows for modifications that enhance the properties of the final product, making it suitable for use in medicinal chemistry and drug discovery research. Overall, this versatile compound plays a fundamental role in expanding the scope of chemical synthesis and fostering innovation in multiple industries.