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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-[(4-fluorophenyl)methyl]-1,3-thiazol-2-amine

Fc1ccc(cc1)Cc1cnc(s1)N Request for Quotation
Chemical Name: 5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-amine
CAS Number: 315241-39-5
Product Number: AG00BZUZ(AGN-PC-0JV683)
Synonyms:
MDL No:
Molecular Formula: C10H9FN2S
Molecular Weight: 208.2553

Identification/Properties

Computed Properties
Molecular Weight:
208.254g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
208.047g/mol
Monoisotopic Mass:
208.047g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
183
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:
H302-H312-H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of 5-(4-Fluorobenzyl)thiazol-2-amine in chemical synthesis lies in its versatility as a building block for the creation of diverse organic molecules. This compound serves as a valuable intermediate in the synthesis of various biologically active compounds and pharmaceutical agents. By incorporating 5-(4-Fluorobenzyl)thiazol-2-amine into synthetic pathways, chemists can access a wide range of structural motifs that exhibit potential medicinal properties. Its unique structure and reactivity make it an essential tool for the construction of complex molecular architectures, contributing significantly to the development of novel compounds with therapeutic potential.