(2-(3-fluoropropoxy)-4-(trifluoroMethoxy)phenyl)boronic acid is a boronic acid derivative featuring a phenyl ring with two distinct alkoxy substituents, one being a 3-fluoropropoxy group and the other a trifluoromethoxy group. This molecule also incorporates a fluorine atom, contributing to its unique chemical properties. It is widely recognized for its role in organic chemistry, particularly as a reagent in the Suzuki-Miyaura cross-coupling reaction, which is a prevalent technique for creating carbon-carbon bonds.
1704073-53-9
Post Buying Request-
-
Basic information
- Product Name: (2-(3-fluoropropoxy)-4-(trifluoroMethoxy)phenyl)boronic acid
- Synonyms: (2-(3-fluoropropoxy)-4-(trifluoroMethoxy)phenyl)boronic acid
- CAS NO:1704073-53-9
- Molecular Formula: C10H11BF4O4
- Molecular Weight: 281.9965528
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1704073-53-9.mol
-
Chemical Properties
- Melting Point: N/A
- Boiling Point: 360.0±52.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.37±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 8.32±0.53(Predicted)
- CAS DataBase Reference: (2-(3-fluoropropoxy)-4-(trifluoroMethoxy)phenyl)boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (2-(3-fluoropropoxy)-4-(trifluoroMethoxy)phenyl)boronic acid(1704073-53-9)
- EPA Substance Registry System: (2-(3-fluoropropoxy)-4-(trifluoroMethoxy)phenyl)boronic acid(1704073-53-9)
-
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: 1704073-53-9(Hazardous Substances Data)
1704073-53-9 Suppliers
Recommended suppliers
1704073-53-9 Usage
Uses
Used in Organic Chemistry:(2-(3-fluoropropoxy)-4-(trifluoroMethoxy)phenyl)boronic acid is utilized as a reagent in the Suzuki-Miyaura cross-coupling reaction for the formation of carbon-carbon bonds. This reaction is highly significant in the synthesis of complex organic molecules, making the boronic acid derivative an essential component in this field.
Used in Medicinal Chemistry and Drug Discovery:
As a versatile reagent, (2-(3-fluoropropoxy)-4-(trifluoroMethoxy)phenyl)boronic acid is also employed in the synthesis of complex organic molecules in medicinal chemistry and drug discovery. Its unique structure and reactivity make it a valuable building block for the development of new pharmaceutical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1704073-53-9 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, 5 and 3 respectively.Calculate Digit Verification of CAS Registry Number 1704073-53:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*7)+(3*3)+(2*5)+(1*3)=139
139 % 10 = 9
So 1704073-53-9 is a valid CAS Registry Number.
1704073-53-9Upstream product
1704073-53-9Downstream Products
Post a RFQ
1
What can I do for you?
Get Best Price
Get Best Price for 1704073-53-9
(2-(3-fluoropropoxy)-4-(trifluoroMethoxy)phenyl)boronic acid
