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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)-

2-Chloro-4-(trifluoromethoxy)benzaldehyde

O=Cc1ccc(cc1Cl)OC(F)(F)F Request for Quotation
Chemical Name: 2-Chloro-4-(trifluoromethoxy)benzaldehyde
CAS Number: 1079351-20-4
Product Number: AG0093ZP(AGN-PC-0WAN6I)
Synonyms:
MDL No: MFCD18393768
Molecular Formula: C8H4ClF3O2
Molecular Weight: 224.5644

Identification/Properties

Computed Properties
Molecular Weight:
224.563g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
223.985g/mol
Monoisotopic Mass:
223.985g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
207
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-4-(trifluoromethoxy)benzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the manufacturing of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique chemical properties.In chemical synthesis, $name$ acts as a valuable intermediate for the synthesis of complex organic molecules. Its chloro and trifluoromethoxy groups enable it to participate in various reactions such as nucleophilic substitutions, acylations, and condensations. These functional groups enhance the reactivity and selectivity of the compound, making it a valuable tool for chemists in creating new molecular structures.One of the notable applications of 2-Chloro-4-(trifluoromethoxy)benzaldehyde is in the synthesis of biologically active compounds. By utilizing this compound as a starting material, chemists can access a wide range of derivatives that exhibit potential pharmacological activities. Additionally, its presence in the synthesis of agrochemicals contributes to the development of novel pesticides and herbicides with improved efficacy and environmental safety profiles.Overall, the strategic role of 2-Chloro-4-(trifluoromethoxy)benzaldehyde in chemical synthesis lies in its versatility and reactivity, enabling the efficient construction of diverse molecular structures with significant importance in various industries.