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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-Propenoic acid, 3-[3-(trifluoromethoxy)phenyl]-

OC(=O)C=Cc1cccc(c1)OC(F)(F)F Request for Quotation
Chemical Name: 2-Propenoic acid, 3-[3-(trifluoromethoxy)phenyl]-
CAS Number: 168833-80-5
Product Number: AG003BAG(AGN-PC-0JVO2Z)
Synonyms:
MDL No:
Molecular Formula: C10H7F3O3
Molecular Weight: 232.1560

Identification/Properties

Properties
Storage:
Room Temperature;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
232.158g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
232.035g/mol
Monoisotopic Mass:
232.035g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
273
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335
Precautionary Statements:
P261-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(3-(Trifluoromethoxy)phenyl)acrylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. Due to its unique molecular structure, it serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials.One of the primary applications of 3-(3-(Trifluoromethoxy)phenyl)acrylic acid in chemical synthesis is as a valuable intermediate in the production of pharmaceutical compounds. Its trifluoromethoxyphenyl group imparts desirable properties such as increased lipophilicity and metabolic stability, making it a preferred structural motif in drug design. By incorporating this compound into the synthesis of pharmaceuticals, researchers can enhance bioavailability, potency, and selectivity of the final products.Moreover, 3-(3-(Trifluoromethoxy)phenyl)acrylic acid plays a crucial role in the development of agrochemicals, particularly herbicides and fungicides. The presence of the trifluoromethoxy group enhances the herbicidal and fungicidal activity of these compounds, making them more effective in controlling unwanted plant growth and fungal diseases. By utilizing this compound in the synthesis of agrochemicals, scientists can create products with improved performance and environmental compatibility.In addition to pharmaceuticals and agrochemicals, 3-(3-(Trifluoromethoxy)phenyl)acrylic acid finds application in the synthesis of advanced materials such as polymers, catalysts, and specialty chemicals. Its structural versatility and unique chemical properties enable the preparation of functionalized materials with tailored physical and chemical characteristics. By incorporating this compound into the production of advanced materials, researchers can develop innovative solutions for various industrial and scientific applications.