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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, 3-(1,1,2,2-tetrafluoroethoxy)-

O=Cc1cccc(c1)OC(C(F)F)(F)F Request for Quotation
Chemical Name: Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-
CAS Number: 35295-35-3
Product Number: AG003HZ2(AGN-PC-0JLM2F)
Synonyms:
MDL No:
Molecular Formula: C9H6F4O2
Molecular Weight: 222.1364

Identification/Properties

Properties
BP:
234 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.454(lit.)
Computed Properties
Molecular Weight:
222.139g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
222.03g/mol
Monoisotopic Mass:
222.03g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
220
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 3-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde is a versatile compound known for its application in chemical synthesis. As a key intermediate in organic chemistry, it serves as a highly valuable building block for the creation of various complex molecules. Its unique structure and properties make it a sought-after reagent in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. By incorporating this compound into reactions, chemists can introduce the 1,1,2,2-tetrafluoroethoxy functional group into target molecules, enabling precise modifications and enhancing desired properties. Furthermore, the presence of the reactive aldehyde group allows for further derivatization, opening up opportunities for the development of novel compounds with tailored functionalities. In summary, the 3-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde plays a crucial role in advancing the field of chemical synthesis by enabling the efficient construction of diverse molecular structures with strategic fluorinated components.