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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, 1-chloro-4-methoxy-2-methyl-

COc1ccc(c(c1)C)Cl Request for Quotation
Chemical Name: Benzene, 1-chloro-4-methoxy-2-methyl-
CAS Number: 13334-71-9
Product Number: AG0014PC(AGN-PC-0JRGGR)
Synonyms:
MDL No: MFCD00086700
Molecular Formula: C8H9ClO
Molecular Weight: 156.6095

Identification/Properties

Properties
BP:
212.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
1.534-1.536
Computed Properties
Molecular Weight:
156.609g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
156.034g/mol
Monoisotopic Mass:
156.034g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
105
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


4-Chloro-3-methylanisole, a versatile compound widely used in chemical synthesis, is a valuable building block in organic chemistry. Its ability to serve as a precursor for various functional groups makes it an essential component in the creation of a range of compounds. In chemical synthesis, this compound plays a crucial role in the formation of complex molecules through reactions such as nucleophilic substitution, Friedel-Crafts acylation, and Suzuki coupling. With its unique structure and reactivity, 4-Chloro-3-methylanisole enables chemists to create diverse and intricate molecular architectures with precision and efficiency.