640292-04-2

Basic information

• Product Name: 5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBALDEHYDE
• Synonyms: 5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBALDEHYDE;SALOR-INT L482803-1EA;5-(4-BROMOPHENYL)-3-ISOXAZOLECARBALDEHYDE;OTAVA-BB 1150845;5-(4-Bromophenyl)-3-isoxazolecarboxaldehyde
• CAS NO: 640292-04-2
• Molecular Formula: C₁₀H₆BrNO₂
• Molecular Weight: 252.06
• Mol File: 640292-04-2.mol

Chemical Properties

• Boiling Point: 409.4±35.0 °C(Predicted)
• Appearance: /
• Density: 1.589±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: -6.43±0.38(Predicted)
• CAS DataBase Reference: 5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBALDEHYDE(640292-04-2)
• EPA Substance Registry System: 5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBALDEHYDE(640292-04-2)

Safety Data

• Hazardous Substances Data: 640292-04-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBALDEHYDE is used as a versatile intermediate in organic synthesis for the creation of diverse organic compounds. Its unique structure allows for the formation of various chemical entities that can be applied across different fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBALDEHYDE is used as a precursor for the development of potential drug candidates. Its presence in the synthesis process aids in the creation of new medicinal compounds that can address various health conditions.
Used in Agrochemical Industry:
5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBALDEHYDE is also utilized as a precursor in the agrochemical industry, where it contributes to the synthesis of compounds that can be used in the development of pesticides, herbicides, and other agricultural chemicals to improve crop protection and yield.
Used in the Synthesis of Bioactive Compounds:
5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBALDEHYDE is used as a key component in the synthesis of bioactive compounds, which have potential applications in medicine and other biological fields. Its structural features facilitate the development of compounds with specific biological activities.

Upstream product

• 33277-15-5 ethyl 5-(4-bromo-phenyl)-isoxazole-3-carboxylate 
• 640291-96-9 [5-(4-bromo-phenyl)-isoxazol-3-yl]-methanol 
• 99-90-1 para-bromoacetophenone 
• 40155-54-2 ethyl 4-(4-bromophenyl)-2,4-dioxobutanoate 

Downstream Products

• 1378938-17-0 2-amino-3-cyano-7-dimethylamino-4-(5-(4-bromophenyl)-isoxazol-3-yl)-4H-chromene 
• 1240306-86-8 1-((5-(4-bromophenyl)isoxazol-3-yl)methyl)azetidine-3-carboxylic acid 
• 640292-10-0 2-{[5-(4-bromophenyl)isoxazol-3-yl]hydroxymethyl}acrylic acid methyl ester 

Relevant articles and documents

2-Amino-3-cyano-4-(5-arylisoxazol-3-yl)-4H-chromenes: Synthesis and in vitro cytotoxic activity

A new series of 4-aryl-4H-chromenes bearing a 5-arylisoxazol-3-yl moiety at the C-4 position were prepared as potential anticancer agents. The in vitro cytotoxic activity of the synthesized compounds was investigated against a panel of tumor cell lines in

Facile Baylis-Hillman Reaction of Substituted 3-Isoxazolecarbaldehydes: The Impact of a Proximal Heteroatom Within a Heterocycle on the Acceleration of the Reaction

The fast and facile Baylis-Hillman reaction in substituted 3-isoxazolecarbaldehydes confirms the impact of the proximal heteroatom within a heterocycle towards enhanced reactivity of the formyl group for this reaction.