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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-(3-FLUOROBENZYL)-1,3-THIAZOL-2-AMINE

Fc1cccc(c1)Cc1cnc(s1)N Request for Quotation
Chemical Name: 5-(3-FLUOROBENZYL)-1,3-THIAZOL-2-AMINE
CAS Number: 884497-40-9
Product Number: AG004JJF(AGN-PC-0WB3AE)
Synonyms:
MDL No:
Molecular Formula: C10H9FN2S
Molecular Weight: 208.2553

Identification/Properties

Properties
Storage:
2-8℃;Light sensitive;Keep in dry area;
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:
191
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(3-Fluorobenzyl)thiazol-2-amine is a versatile compound widely utilized in chemical synthesis as a building block for pharmaceutical and agrochemical products. Its unique structural properties make it a valuable intermediate in the development of various complex organic molecules. This compound serves as a key component in the synthesis of potential therapeutics, such as anti-cancer drugs and antimicrobial agents. Additionally, it is utilized in the creation of novel materials with specialized properties, contributing to advancements in materials science. The application of 5-(3-Fluorobenzyl)thiazol-2-amine in chemical synthesis plays a crucial role in expanding the scope of organic chemistry and driving innovation in the pharmaceutical and agricultural industries.