[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid is a boronic acid derivative with the molecular formula C4H7BO4, characterized by the presence of a boronic acid group, a prop-1-en-1-yl group, and functional groups such as methoxy and oxo. This versatile chemical compound is widely utilized in organic synthesis and medicinal chemistry.
290305-47-4
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Basic information
- Product Name: [(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid
- Synonyms: [(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid
- CAS NO:290305-47-4
- Molecular Formula:
- Molecular Weight: 129.908
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: [(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: [(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid(290305-47-4)
- EPA Substance Registry System: [(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid(290305-47-4)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 290305-47-4(Hazardous Substances Data)
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290305-47-4 Usage
Uses
Used in Organic Synthesis:[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid is used as a reagent in Suzuki coupling reactions, which are crucial for the formation of carbon-carbon bonds. These reactions are essential in constructing complex organic molecules and are particularly valuable in the synthesis of pharmaceuticals and natural products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid has demonstrated potential as an anticancer agent. Studies have shown that [(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid can inhibit the growth of cancer cells, making it a promising candidate for further research and development in cancer therapeutics.
Used in Pharmaceutical Industry:
[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity enable the creation of novel drug candidates with potential applications in treating a range of diseases and conditions.
Used in Research and Development:
This boronic acid derivative is also employed in research and development settings, where it serves as a valuable tool for exploring new chemical reactions and understanding the underlying mechanisms. Its use in this context contributes to the advancement of knowledge in organic chemistry and medicinal chemistry, ultimately leading to the discovery of new compounds with therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 290305-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,3,0 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.Calculate Digit Verification of CAS Registry Number 290305-47:
(8*2)+(7*9)+(6*0)+(5*3)+(4*0)+(3*5)+(2*4)+(1*7)=124
124 % 10 = 4
So 290305-47-4 is a valid CAS Registry Number.
290305-47-4Upstream product
290305-47-4Downstream Products
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[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]boronic acid
