(2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid is a boronic acid derivative with a molecular formula of C14H21BNO5S. It features a sulfonyl group and a piperidinyl group attached to a phenyl ring, giving it unique structural and reactivity properties.
Used in Organic Synthesis:
(2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid is used as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds. Its application is particularly valuable in the construction of biologically active molecules and pharmaceuticals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid serves as a key component in the development of new drugs. Its unique structure and reactivity make it instrumental in creating complex organic molecules with potential biological activity.
Used in Chemical Biology Research:
(2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid also plays a role in chemical biology research, where it is utilized as a tool to explore and understand the interactions between biological systems and synthetic compounds.
Used in Organic Synthesis:
(2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid is used as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds. Its application is particularly valuable in the construction of biologically active molecules and pharmaceuticals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid serves as a key component in the development of new drugs. Its unique structure and reactivity make it instrumental in creating complex organic molecules with potential biological activity.
Used in Chemical Biology Research:
(2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid also plays a role in chemical biology research, where it is utilized as a tool to explore and understand the interactions between biological systems and synthetic compounds.
1704080-74-9
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Basic information
- Product Name: (2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid
- Synonyms: (2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid
- CAS NO:1704080-74-9
- Molecular Formula: C13H20BNO5S
- Molecular Weight: 313.1776
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704080-74-9.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 527.1±60.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.33±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 7.68±0.58(Predicted)
- CAS DataBase Reference: (2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid(1704080-74-9)
- EPA Substance Registry System: (2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid(1704080-74-9)
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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: 1704080-74-9(Hazardous Substances Data)
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1704080-74-9 Usage
Check Digit Verification of cas no
The CAS Registry Mumber 1704080-74-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,8 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.Calculate Digit Verification of CAS Registry Number 1704080-74:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*8)+(3*0)+(2*7)+(1*4)=139
139 % 10 = 9
So 1704080-74-9 is a valid CAS Registry Number.
1704080-74-9Upstream product
1704080-74-9Downstream Products
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(2-Methoxy-5-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid
