1. Home
  2. Benzaldehyde, 2-fluoro-6-methoxy-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

Benzaldehyde, 2-fluoro-6-methoxy-

COc1cccc(c1C=O)F Request for Quotation
Chemical Name: Benzaldehyde, 2-fluoro-6-methoxy-
CAS Number: 146137-74-8
Product Number: AG001DQ3(AGN-PC-0KK8GV)
Synonyms:
MDL No:
Molecular Formula: C8H7FO2
Molecular Weight: 154.1384

Identification/Properties

Properties
MP:
59-63 °C(lit.)
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Stability:
Air Sensitive
Refractive Index:
n20/D 1.339
Computed Properties
Molecular Weight:
154.14g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
154.043g/mol
Monoisotopic Mass:
154.043g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
138
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

Request for Quotation

Customer Feedback

Chemical Structure


2-Fluoro-6-methoxybenzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique chemical properties.In chemical synthesis, 2-Fluoro-6-methoxybenzaldehyde acts as a crucial intermediate in the preparation of biologically active molecules. Its fluorine substitution provides enhanced reactivity and selectivity in organic reactions, making it valuable for the incorporation of fluorine atoms into complex organic frameworks.Furthermore, the methoxy group present in 2-Fluoro-6-methoxybenzaldehyde plays a significant role in modulating the compound's electronic properties, influencing its solubility and interactions with other molecules during synthesis. This functional group also enables the compound to participate in various transformations, such as nucleophilic substitution and aromatic ring substitutions.Overall, the application of 2-Fluoro-6-methoxybenzaldehyde in chemical synthesis showcases its importance as a versatile and indispensable building block for the creation of diverse chemical entities with potential applications in pharmaceutical, agricultural, and other industries.