1. Home
  2. Benzenamine, 2-bromo-4-chloro-5-methoxy-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-bromo-4-chloro-5-methoxy-

COc1cc(N)c(cc1Cl)Br Request for Quotation
Chemical Name: Benzenamine, 2-bromo-4-chloro-5-methoxy-
CAS Number: 98446-57-2
Product Number: AG00IK3B(AGN-PC-002IOG)
Synonyms:
MDL No:
Molecular Formula: C7H7BrClNO
Molecular Weight: 236.4936

Identification/Properties

Computed Properties
Molecular Weight:
236.493g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
234.94g/mol
Monoisotopic Mass:
234.94g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Bromo-4-chloro-5-methoxyaniline is a versatile chemical compound widely used in chemical synthesis processes. This compound serves as a valuable building block in the preparation of various organic molecules and is particularly instrumental in the development of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactive properties make it a valuable intermediate for the synthesis of complex compounds with diverse applications. In chemical synthesis, 2-Bromo-4-chloro-5-methoxyaniline can undergo various reactions such as nucleophilic substitution, Suzuki coupling, and lithiation reactions to introduce specific functional groups or modify its chemical structure, allowing chemists to tailor the compound for specific target molecules. Additionally, the presence of both bromine and chlorine atoms in the compound's structure enhances its versatility in participating in diverse chemical transformations. Chemical synthesis strategies utilizing 2-Bromo-4-chloro-5-methoxyaniline enable the efficient and controlled production of valuable compounds with wide-ranging applications in the fields of medicine, agriculture, and materials science.