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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)-

5-Thiazolemethanol, 2-[3-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-

OCc1sc(nc1C)c1ccc(c(c1)F)C(F)(F)F Request for Quotation
Chemical Name: 5-Thiazolemethanol, 2-[3-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-
CAS Number: 317319-27-0
Product Number: AG00C9X1(AGN-PC-01XG51)
Synonyms:
MDL No:
Molecular Formula: C12H9F4NOS
Molecular Weight: 291.2646

Identification/Properties

Properties
MP:
157-159ºC
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
291.264g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
2
Exact Mass:
291.034g/mol
Monoisotopic Mass:
291.034g/mol
Topological Polar Surface Area:
61.4A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
315
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2-(3-Fluoro-4-(trifluoromethyl)phenyl)-4-methylthiazol-5-yl)methanol is a versatile building block in chemical synthesis due to its unique structural features. It serves as a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and functional materials. By incorporating this compound into reaction schemes, chemists can introduce specific functionalities and stereochemical elements into target molecules, enabling precise control over the synthesis process. Furthermore, the presence of the fluoro, trifluoromethyl, and thiazolyl groups offers opportunities for further derivatization through selective chemical transformations, providing access to a diverse array of compounds with tailored properties.