[7-(dihydroxyboranyl)pyren-2-yl]boronic acid is a chemical compound belonging to the class of boronic acids, characterized by a pyrene molecule with a boronic acid group attached to it. [7-(dihydroxyboranyl)pyren-2-yl]boronic acid is known for its unique properties due to the presence of the boron atom, which makes it valuable in the development of new materials and pharmaceutical compounds.
1099731-44-8
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Basic information
- Product Name: [7-(dihydroxyboranyl)pyren-2-yl]boronic acid
- Synonyms: [7-(dihydroxyboranyl)pyren-2-yl]boronic acid
- CAS NO:1099731-44-8
- Molecular Formula:
- Molecular Weight: 289.891
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1099731-44-8.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 641.4±65.0 °C(Predicted)
- Flash Point: N/A
- Appearance: N/A
- Density: 1.46±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: [7-(dihydroxyboranyl)pyren-2-yl]boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: [7-(dihydroxyboranyl)pyren-2-yl]boronic acid(1099731-44-8)
- EPA Substance Registry System: [7-(dihydroxyboranyl)pyren-2-yl]boronic acid(1099731-44-8)
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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: 1099731-44-8(Hazardous Substances Data)
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1099731-44-8 Usage
Uses
Used in Organic Synthesis:[7-(dihydroxyboranyl)pyren-2-yl]boronic acid is used as a reagent in organic synthesis for various reactions, particularly the Suzuki-Miyaura coupling. This coupling method is widely utilized for forming carbon-carbon bonds, and the boronic acid group in [7-(dihydroxyboranyl)pyren-2-yl]boronic acid allows it to participate in these reactions by reacting with aryl halides or pseudohalides.
Used in Pharmaceutical Compound Development:
The unique properties of [7-(dihydroxyboranyl)pyren-2-yl]boronic acid, conferred by the presence of the boron atom, make it a promising candidate for the development of new pharmaceutical compounds. Its versatility in participating in various chemical reactions and processes contributes to its significance in the field of organic chemistry.
Used in Material Science:
[7-(dihydroxyboranyl)pyren-2-yl]boronic acid's unique properties also make it useful in the development of new materials, where its ability to form carbon-carbon bonds and its reactivity with aryl halides or pseudohalides can be exploited to create novel materials with specific characteristics and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1099731-44-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,9,7,3 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.Calculate Digit Verification of CAS Registry Number 1099731-44:
(9*1)+(8*0)+(7*9)+(6*9)+(5*7)+(4*3)+(3*1)+(2*4)+(1*4)=188
188 % 10 = 8
So 1099731-44-8 is a valid CAS Registry Number.
1099731-44-8Upstream product
1099731-44-8Downstream Products
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[7-(dihydroxyboranyl)pyren-2-yl]boronic acid
