1. Home
  2. [2-(3-bromophenyl)-1,3-oxazol-4-yl]methanol

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

[2-(3-bromophenyl)-1,3-oxazol-4-yl]methanol

OCc1coc(n1)c1cccc(c1)Br Request for Quotation
Chemical Name: [2-(3-bromophenyl)-1,3-oxazol-4-yl]methanol
CAS Number: 885272-67-3
Product Number: AG00472Z(AGN-PC-0J0YDM)
Synonyms:
MDL No:
Molecular Formula: C10H8BrNO2
Molecular Weight: 254.0800

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The chemical compound (2-(3-Bromophenyl)oxazol-4-yl)methanol, also known as $name$, is a versatile building block in chemical synthesis. It is commonly utilized as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals.$name$ serves as a valuable starting material for the synthesis of organic molecules due to its unique structural properties. Its oxazole ring provides opportunities for functional group manipulation, enabling the introduction of different substituents to tailor the compound's properties for specific applications.In chemical synthesis, $name$ can undergo various reactions such as nucleophilic substitutions, acylations, and reductions to yield structurally diverse compounds. Its bromophenyl group can serve as a handle for further derivatization, allowing for the creation of complex molecules with specific biological or chemical activities.Overall, the application of (2-(3-Bromophenyl)oxazol-4-yl)methanol in chemical synthesis exemplifies its importance as a versatile building block for the construction of multifunctional molecules with potential benefits in the fields of pharmaceuticals, materials science, and agrochemicals.