(3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid is a boronic acid derivative with the molecular formula C9H10BClFO3. It features a phenyl ring substituted with a chloro group and a 3-fluoropropoxy group, with the boronic acid group attached. (3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid is recognized for its utility in organic synthesis and medicinal chemistry, serving as a valuable building block in the creation of pharmaceuticals, agrochemicals, and materials.
1704080-24-9
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Basic information
- Product Name: (3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid
- Synonyms: (3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid
- CAS NO:1704080-24-9
- Molecular Formula: C9H11BClFO3
- Molecular Weight: 232.4442432
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704080-24-9.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid(1704080-24-9)
- EPA Substance Registry System: (3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid(1704080-24-9)
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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: 1704080-24-9(Hazardous Substances Data)
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1704080-24-9 Usage
Uses
Used in Organic Synthesis:(3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid is used as a reagent in organic synthesis for its ability to form stable complexes with diols and other nucleophiles. This characteristic makes it an important tool in developing new chemical reactions and processes.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid is utilized as a building block in the synthesis of pharmaceuticals. Its unique structure, including the boronic acid and fluoropropoxy groups, allows for the development of compounds with specific biological activities.
Used in the Synthesis of Agrochemicals:
(3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid is also employed in the synthesis of agrochemicals, where its reactivity and complex-forming ability with various nucleophiles contribute to the creation of effective compounds for agricultural applications.
Used in Materials Science:
(3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid finds application in materials science, where its properties can be leveraged to develop new materials with tailored characteristics, potentially useful in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1704080-24-9 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, 2 and 4 respectively.Calculate Digit Verification of CAS Registry Number 1704080-24:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*8)+(3*0)+(2*2)+(1*4)=129
129 % 10 = 9
So 1704080-24-9 is a valid CAS Registry Number.
1704080-24-9Upstream product
1704080-24-9Downstream Products
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(3-chloro-4-(3-fluoropropoxy)phenyl)boronic acid
