3-Isoxazolecarboxaldehyde, 5-(4-bromophenyl)-


Chemical Name: 3-Isoxazolecarboxaldehyde, 5-(4-bromophenyl)-
CAS Number: 640292-04-2
Product Number: AG003M58(AGN-PC-008E8U)
Synonyms:
MDL No:
Molecular Formula: C10H6BrNO2
Molecular Weight: 252.0641

Identification/Properties


Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
252.067g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
250.958g/mol
Monoisotopic Mass:
250.958g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
204
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-(4-Bromophenyl)isoxazole-3-carbaldehyde is a versatile organic compound widely employed in chemical synthesis as a key building block. This compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity. It serves as a valuable intermediate in the synthesis of heterocyclic compounds with diverse functionalities, making it suitable for the development of new drug candidates and molecular probes. Additionally, 5-(4-Bromophenyl)isoxazole-3-carbaldehyde is utilized in the preparation of advanced materials such as liquid crystals and polymers, contributing to the advancement of materials science. Its ability to undergo various chemical transformations, including condensation reactions and functional group modifications, underscores its significance in organic synthesis and highlights its importance in the field of chemistry.