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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)-

4-Chloro-2-fluoro-3-methoxyphenylboronic acid

COc1c(Cl)ccc(c1F)B(O)O Request for Quotation
Chemical Name: 4-Chloro-2-fluoro-3-methoxyphenylboronic acid
CAS Number: 944129-07-1
Product Number: AG00367R(AGN-PC-0WAA7O)
Synonyms:
MDL No:
Molecular Formula: C7H7BClFO3
Molecular Weight: 204.3911

Identification/Properties

Properties
BP:
487.6±40.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
204.388g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
204.016g/mol
Monoisotopic Mass:
204.016g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-2-fluoro-3-methoxyphenylboronic acid is a versatile compound widely used in chemical synthesis. Its primary application lies in its role as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. With its distinct chemical structure, this compound serves as a key intermediate in the synthesis of biologically active molecules and complex organic compounds. By incorporating 4-Chloro-2-fluoro-3-methoxyphenylboronic acid into synthetic pathways, chemists can efficiently construct new molecules with specific properties and functionalities, making it a crucial asset in modern organic chemistry research and development. Its unique properties make it a powerful tool for creating innovative compounds with diverse applications across industries.