(4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid is a boronic acid derivative with the molecular formula C13H18BClN2O2. It features a phenyl ring with a chlorine atom at the 4-position and a boronic acid functional group at the 3-position, along with a 4-methylpiperazin-1-ylmethyl group attached to the phenyl ring. This chemical compound is known for its potential applications in medicinal and pharmaceutical research, as well as in organic chemistry, due to its ability to form covalent bonds with specific biological molecules and its reactivity with diols and other nucleophiles.
1704073-61-9
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Basic information
- Product Name: (4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid
- Synonyms: (4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid
- CAS NO:1704073-61-9
- Molecular Formula: C12H18BClN2O2
- Molecular Weight: 268.54752
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704073-61-9.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 420.5±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.27±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 8.32±0.10(Predicted)
- CAS DataBase Reference: (4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid(1704073-61-9)
- EPA Substance Registry System: (4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid(1704073-61-9)
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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: 1704073-61-9(Hazardous Substances Data)
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1704073-61-9 Usage
Uses
Used in Medicinal and Pharmaceutical Research:(4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid is used as a chemical tool for drug development and chemical biology studies. Its ability to form covalent bonds with certain biological molecules makes it a valuable asset in the design and synthesis of new drugs targeting specific biological pathways.
Used in Organic Chemistry:
In the field of organic chemistry, (4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid is used as a reagent for its capacity to bind with diols and other nucleophiles. This property is crucial in various chemical reactions and synthesis processes, contributing to the development of new compounds and materials.
Used in Chemical Biology Studies:
(4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid is also utilized in chemical biology research to understand the interactions between small molecules and biological systems. Its unique structure and reactivity allow for the exploration of novel biochemical pathways and the potential discovery of new therapeutic targets.
Check Digit Verification of cas no
The CAS Registry Mumber 1704073-61-9 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 3 respectively; the second part has 2 digits, 6 and 1 respectively.Calculate Digit Verification of CAS Registry Number 1704073-61:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*7)+(3*3)+(2*6)+(1*1)=139
139 % 10 = 9
So 1704073-61-9 is a valid CAS Registry Number.
1704073-61-9Upstream product
1704073-61-9Downstream Products
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(4-chloro-3-((4-Methylpiperazin-1-yl)Methyl)phenyl)boronic acid
