(3-chloro-4-((diethylamino)methyl)phenyl)boronic acid is a chemical compound that features a boronic acid functional group, a chloro substituent, and a diethylamino group. This versatile molecule is widely utilized in organic synthesis and pharmaceutical research, serving as a reagent for crafting biologically active molecules and as a fundamental building block in drug development. The boronic acid component is particularly notable for its ability to form stable complexes with diols and other electron-rich species, which is advantageous for a range of cross-coupling reactions, including the renowned Suzuki-Miyaura coupling reactions. The incorporation of the diethylamino group further expands the molecule's synthetic potential, offering additional avenues for functionalization and chemical manipulation.
1704074-24-7
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Basic information
- Product Name: (3-chloro-4-((diethylaMino)Methyl)phenyl)boronic acid
- Synonyms: (3-chloro-4-((diethylaMino)Methyl)phenyl)boronic acid
- CAS NO:1704074-24-7
- Molecular Formula: C11H17BClNO2
- Molecular Weight: 241.52218
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704074-24-7.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 360.0±52.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.16±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 7.40±0.17(Predicted)
- CAS DataBase Reference: (3-chloro-4-((diethylaMino)Methyl)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-chloro-4-((diethylaMino)Methyl)phenyl)boronic acid(1704074-24-7)
- EPA Substance Registry System: (3-chloro-4-((diethylaMino)Methyl)phenyl)boronic acid(1704074-24-7)
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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: 1704074-24-7(Hazardous Substances Data)
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1704074-24-7 Usage
Uses
Used in Organic Synthesis:(3-chloro-4-((diethylamino)methyl)phenyl)boronic acid is used as a reagent for the synthesis of biologically active molecules due to its ability to form stable complexes with electron-rich species, facilitating various cross-coupling reactions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-chloro-4-((diethylamino)methyl)phenyl)boronic acid is used as a building block for drug development, capitalizing on its functional groups to create novel and potentially effective therapeutic agents.
Used in Suzuki-Miyaura Coupling Reactions:
(3-chloro-4-((diethylaMino)Methyl)phenyl)boronic acid is utilized as a key participant in Suzuki-Miyaura coupling reactions, a widely used method in organic chemistry for the formation of carbon-carbon bonds, particularly valuable in the synthesis of complex organic and medicinal molecules.
Used for Further Functionalization in Synthetic Chemistry:
The presence of the diethylamino group in (3-chloro-4-((diethylamino)methyl)phenyl)boronic acid allows for additional functionalization, making it a useful intermediate for the creation of a diverse array of chemical entities in synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1704074-24-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,7 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.Calculate Digit Verification of CAS Registry Number 1704074-24:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*7)+(3*4)+(2*2)+(1*4)=137
137 % 10 = 7
So 1704074-24-7 is a valid CAS Registry Number.
1704074-24-7Upstream product
1704074-24-7Downstream Products
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(3-chloro-4-((diethylaMino)Methyl)phenyl)boronic acid
