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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)-

Benzaldehyde, 2,4-difluoro-5-methoxy-

COc1cc(C=O)c(cc1F)F Request for Quotation
Chemical Name: Benzaldehyde, 2,4-difluoro-5-methoxy-
CAS Number: 177034-25-2
Product Number: AG00252W(AGN-PC-0BWPHL)
Synonyms:
MDL No: MFCD24539280
Molecular Formula: C8H6F2O2
Molecular Weight: 172.1288

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
172.131g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
172.034g/mol
Monoisotopic Mass:
172.034g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
163
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
Precautionary Statements:
P261-P280-P305+P351+P338-P304+P340-P405-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Difluoro-5-methoxybenzaldehyde is a versatile compound widely used in chemical synthesis for its unique properties. This aldehyde is particularly valued for its role as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its presence of both fluorine and methoxy functional groups provides distinctive reactivity and selectivity in organic reactions. In the field of medicinal chemistry, 2,4-Difluoro-5-methoxybenzaldehyde is often utilized in the synthesis of drug candidates due to its ability to introduce specific structural motifs that can enhance the biological activity or selectivity of the final compound. Additionally, in agrochemical research, this compound has shown promise in developing new crop protection agents with improved efficacy and safety profiles. Overall, the application of 2,4-Difluoro-5-methoxybenzaldehyde in chemical synthesis is pivotal for the advancement of various industries reliant on the design and production of novel molecules with tailored properties and functions.