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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)-

Phenol, 2-methoxy-5-(trifluoromethyl)-

COc1ccc(cc1O)C(F)(F)F Request for Quotation
Chemical Name: Phenol, 2-methoxy-5-(trifluoromethyl)-
CAS Number: 349-67-7
Product Number: AG00CMC6(AGN-PC-006ZEQ)
Synonyms:
MDL No:
Molecular Formula: C8H7F3O2
Molecular Weight: 192.1351896

Identification/Properties

Computed Properties
Molecular Weight:
192.137g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
192.04g/mol
Monoisotopic Mass:
192.04g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
169
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:
Danger
UN#:
3265
Hazard Statements:
H302-H315-H318-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methoxy-5-(trifluoromethyl)phenol, also known as $name$, is a versatile compound commonly used in chemical synthesis. This compound plays a crucial role in the production of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties.In chemical synthesis, 2-Methoxy-5-(trifluoromethyl)phenol serves as a valuable building block for the creation of more complex molecules. Its trifluoromethyl group imparts enhanced chemical reactivity and stability, making it a desirable reagent in organic reactions. This compound is often employed in the synthesis of biologically active compounds, such as pharmaceutical intermediates and herbicides, where the trifluoromethyl group can impart desirable properties like increased lipophilicity and metabolic stability.Furthermore, the methoxy group in 2-Methoxy-5-(trifluoromethyl)phenol provides additional versatility in chemical transformations, allowing for the introduction of various functional groups to fine-tune the properties of the final products. This compound's application in chemical synthesis extends to the development of new materials with specialized properties, such as polymers, dyes, and catalysts.Overall, 2-Methoxy-5-(trifluoromethyl)phenol is a valuable tool in the hands of chemists and researchers, enabling the synthesis of diverse compounds with tailored properties for a wide range of applications.