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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)-

4-Thiazolemethanol, 5-bromo-

OCc1ncsc1Br Request for Quotation
Chemical Name: 4-Thiazolemethanol, 5-bromo-
CAS Number: 912639-68-0
Product Number: AG01C40M(AGN-PC-0CS0QT)
Synonyms:
MDL No:
Molecular Formula: C4H4BrNOS
Molecular Weight: 194.0497

Identification/Properties

Computed Properties
Molecular Weight:
194.046g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
192.92g/mol
Monoisotopic Mass:
192.92g/mol
Topological Polar Surface Area:
61.4A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
82.4
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


(5-Bromothiazol-4-yl)methanol, also known as $name$, is a versatile chemical compound that finds significant application in chemical synthesis. With its unique structure and reactivity, this compound serves as a valuable building block in the synthesis of various organic molecules and pharmaceutical compounds. $name$ can be utilized as a key intermediate in the preparation of diverse functionalized thiazole derivatives, owing to its ability to undergo various chemical transformations. It can participate in reactions such as nucleophilic substitutions, reductions, and cross-coupling reactions to introduce different functional groups onto the thiazole ring. Moreover, $name$ acts as an important precursor for the synthesis of bioactive compounds and pharmaceuticals due to its thiazole moiety, which is a common structural motif in many biologically active molecules. Its incorporation into drug molecules can impart desirable pharmacological properties such as antimicrobial, anticancer, and antiviral activities.In summary, the strategic use of (5-Bromothiazol-4-yl)methanol in chemical synthesis provides chemists with a valuable tool for accessing structurally diverse compounds and developing novel pharmaceutical agents.