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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)-

Benzene, 4-(bromomethyl)-2-chloro-1-methoxy-

BrCc1ccc(c(c1)Cl)OC Request for Quotation
Chemical Name: Benzene, 4-(bromomethyl)-2-chloro-1-methoxy-
CAS Number: 320407-92-9
Product Number: AG003K6I(AGN-PC-009R69)
Synonyms:
MDL No:
Molecular Formula: C8H8BrClO
Molecular Weight: 235.5055

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
235.505g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
233.945g/mol
Monoisotopic Mass:
233.945g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
121
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:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Bromomethyl)-2-chloro-1-methoxybenzene is a versatile compound widely used in chemical synthesis as a key building block for the creation of various organic molecules. This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for selective functional group transformations through various chemical reactions, making it a valuable tool for organic chemists. Additionally, the presence of both a bromomethyl and chloro group in its structure provides opportunities for further derivatization, enabling the synthesis of more complex and diverse chemical structures. In chemical synthesis, 4-(Bromomethyl)-2-chloro-1-methoxybenzene plays a crucial role in the construction of complex molecules with specific functionalities and properties.