(3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid is a chemical compound that features a boronic acid functional group and a chloro-substituted phenyl ring. It also incorporates a pyrrolidin-1-yl group connected to the phenyl ring through a propoxy linker. (3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid is recognized for its versatility in organic synthesis and holds significant value in pharmaceutical and medicinal chemistry due to its potential to form carbon-carbon bonds and its possible biological activity.
1704074-32-7
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Basic information
- Product Name: (3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid
- Synonyms: (3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid
- CAS NO:1704074-32-7
- Molecular Formula: C13H19BClNO3
- Molecular Weight: 283.55886
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704074-32-7.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 469.5±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.25±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 7.66±0.17(Predicted)
- CAS DataBase Reference: (3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid(1704074-32-7)
- EPA Substance Registry System: (3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid(1704074-32-7)
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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: 1704074-32-7(Hazardous Substances Data)
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1704074-32-7 Usage
Uses
Used in Pharmaceutical and Medicinal Chemistry:(3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid serves as a key building block in the synthesis of complex molecules, which is crucial for developing new drugs and pharmacological tools. Its ability to engage in various reactions to form carbon-carbon bonds makes it an essential component in creating intricate molecular structures.
Used in Organic Synthesis:
In the realm of organic synthesis, (3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid is utilized for its reactivity and functional group compatibility, allowing for the creation of a wide array of chemical products and intermediates that can be further used in different applications.
Used in Drug Discovery and Development:
The presence of the pyrrolidin-1-yl group in (3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid may confer specific biological activity, enhancing its potential as a drug candidate or a tool in pharmacological research. This makes it a valuable asset in the early stages of drug discovery and development, where novel and effective compounds are sought to address various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1704074-32-7 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, 3 and 2 respectively.Calculate Digit Verification of CAS Registry Number 1704074-32:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*7)+(3*4)+(2*3)+(1*2)=137
137 % 10 = 7
So 1704074-32-7 is a valid CAS Registry Number.
1704074-32-7Upstream product
1704074-32-7Downstream Products
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(3-chloro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)boronic acid
