Cyclohexylboronic Acid Diethanolamine Ester, a specialized boronic acid, is an essential reagent in the realm of organic chemistry. With a molecular formula of C12H27BNO4, this clear liquid compound is widely utilized in various chemical reactions, particularly in the Suzuki coupling process, making it a valuable tool for chemists. However, due to its potential to cause skin, eye, and respiratory irritation, careful handling is required to ensure safety.
122035-40-9
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Basic information
- Product Name: CYCLOHEXYLBORONIC ACID DIETHANOLAMINE ESTER
- Synonyms: CYCLOHEXYLBORONIC ACID DIETHANOLAMINE ESTER;2-Cyclohexyl-1,3,6,2-dioxazaborocane
- CAS NO:122035-40-9
- Molecular Formula: C10H20BNO2
- Molecular Weight: 197.08
- EINECS: N/A
- Product Categories: Boronic acid
- Mol File: 122035-40-9.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 368.773°C at 760 mmHg
- Flash Point: 176.828°C
- Appearance: /
- Density: 1.039g/cm3
- Vapor Pressure: 0mmHg at 25°C
- Refractive Index: 1.474
- Storage Temp.: 2-8°C
- Solubility: N/A
- CAS DataBase Reference: CYCLOHEXYLBORONIC ACID DIETHANOLAMINE ESTER(CAS DataBase Reference)
- NIST Chemistry Reference: CYCLOHEXYLBORONIC ACID DIETHANOLAMINE ESTER(122035-40-9)
- EPA Substance Registry System: CYCLOHEXYLBORONIC ACID DIETHANOLAMINE ESTER(122035-40-9)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: IRRITANT
- PackingGroup: N/A
- Hazardous Substances Data: 122035-40-9(Hazardous Substances Data)
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122035-40-9 Usage
Uses
Used in Organic Chemistry:Cyclohexylboronic Acid Diethanolamine Ester is used as a reagent for facilitating various chemical reactions in the field of organic chemistry. Its primary application is in the Suzuki coupling, a widely used method for the formation of carbon-carbon bonds, which is crucial for the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Cyclohexylboronic Acid Diethanolamine Ester is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to form carbon-carbon bonds makes it an indispensable component in the development of new drugs and the modification of existing ones.
Used in Material Science:
Cyclohexylboronic Acid Diethanolamine Ester is also utilized in material science for the synthesis of novel materials with unique properties. Its role in creating carbon-carbon bonds allows for the development of advanced materials with improved performance characteristics, such as enhanced stability, reactivity, or selectivity.
Used in Research and Development:
In research and development settings, Cyclohexylboronic Acid Diethanolamine Ester is employed as a versatile reagent for exploring new chemical reactions and mechanisms. Its application in the Suzuki coupling and other reactions provides researchers with a valuable tool for investigating the properties and potential applications of newly synthesized compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 122035-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,0,3 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.Calculate Digit Verification of CAS Registry Number 122035-40:
(8*1)+(7*2)+(6*2)+(5*0)+(4*3)+(3*5)+(2*4)+(1*0)=69
69 % 10 = 9
So 122035-40-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H22BNO3/c13-8-6-12-7-9-15-11(14)10-4-2-1-3-5-10/h10,12-14H,1-9H2
122035-40-9Upstream product
122035-40-9Downstream Products
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CYCLOHEXYLBORONIC ACID DIETHANOLAMINE ESTER
