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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)-

1-(chloromethyl)-4-(difluoromethoxy)benzene

ClCc1ccc(cc1)OC(F)F Request for Quotation
Chemical Name: 1-(chloromethyl)-4-(difluoromethoxy)benzene
CAS Number: 41772-09-2
Product Number: AG019WJG(AGN-PC-002CHO)
Synonyms:
MDL No: MFCD11156112
Molecular Formula: C8H7ClF2O
Molecular Weight: 192.5904

Identification/Properties

Computed Properties
Molecular Weight:
192.59g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
192.015g/mol
Monoisotopic Mass:
192.015g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
124
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


1-(Chloromethyl)-4-(difluoromethoxy)benzene is a versatile compound commonly employed in chemical synthesis due to its unique reactivity and structural properties. This compound acts as a key building block in organic synthesis, specifically in the formation of complex molecules and pharmaceutical intermediates. Its chloromethyl group serves as a reactive site for nucleophilic substitution reactions, allowing for the introduction of different functional groups. Additionally, the presence of the difluoromethoxy group enhances the compound's stability and lipophilicity, making it suitable for use in drug discovery and medicinal chemistry research. Overall, 1-(Chloromethyl)-4-(difluoromethoxy)benzene is a valuable tool in the synthesis of various organic compounds with potential applications in the pharmaceutical industry and material science.