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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)-

2,3-dichloro-N-methylaniline;hydrochloride

CNc1cccc(c1Cl)Cl.Cl Request for Quotation
Chemical Name: 2,3-dichloro-N-methylaniline;hydrochloride
CAS Number: 1187386-16-8
Product Number: AG0090FI(AGN-PC-07HC7F)
Synonyms:
MDL No: MFCD12912804
Molecular Formula: C7H8Cl3N
Molecular Weight: 212.5041

Identification/Properties

Computed Properties
Molecular Weight:
212.498g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
210.972g/mol
Monoisotopic Mass:
210.972g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
108
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3-Dichloro-N-methylaniline hydrochloride is a valuable compound used in chemical synthesis for its unique reactivity and properties. This compound plays a crucial role in various organic transformations, particularly in the formation of complex molecules and pharmaceutical intermediates. Its ability to undergo selective chlorination reactions makes it a versatile building block in the synthesis of a wide range of organic compounds. Additionally, the presence of the N-methyl group enhances its stability and influences its reactivity in specific chemical reactions. The hydrochloride salt form of this compound offers advantages in solubility and handling during synthesis processes. Overall, 2,3-Dichloro-N-methylaniline hydrochloride is a key component in the arsenal of synthetic chemists for creating novel compounds and advancing research in the field of organic chemistry.