(N-Methyl-N-phenylamino)ethylphenylborane is a boron-based reagent that belongs to the class of organoboron compounds. It is known for its ability to act as a nucleophile in various reactions, including the Suzuki-Miyaura coupling and the Stille coupling. Its unique structure, containing both boron and nitrogen atoms, allows it to participate in a wide range of synthetic transformations, making it a valuable tool for the preparation of various organic molecules. Additionally, (N-Methyl-N-phenylamino)ethylphenylborane is often used in pharmaceutical research and drug discovery due to its versatility and the potential to create complex molecular structures.
39967-40-3
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Basic information
- Product Name: (N-Methyl-N-phenylamino)ethylphenylborane
- Synonyms: (N-Methyl-N-phenylamino)ethylphenylborane
- CAS NO:39967-40-3
- Molecular Formula: C15H18BN
- Molecular Weight: 223.12
- EINECS: N/A
- Product Categories: N/A
- Mol File: 39967-40-3.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: (N-Methyl-N-phenylamino)ethylphenylborane(CAS DataBase Reference)
- NIST Chemistry Reference: (N-Methyl-N-phenylamino)ethylphenylborane(39967-40-3)
- EPA Substance Registry System: (N-Methyl-N-phenylamino)ethylphenylborane(39967-40-3)
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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: 39967-40-3(Hazardous Substances Data)
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39967-40-3 Usage
Uses
Used in Pharmaceutical Research and Drug Discovery:(N-Methyl-N-phenylamino)ethylphenylborane is used as a synthetic reagent for the creation of complex molecular structures. Its versatility in participating in various synthetic transformations makes it a valuable tool in the development of new pharmaceutical compounds.
Used in Organic Synthesis:
(N-Methyl-N-phenylamino)ethylphenylborane is used as a nucleophile in the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure allows it to be employed in a wide range of synthetic transformations, contributing to the development of diverse organic molecules.
Used in the Suzuki-Miyaura Coupling:
(N-Methyl-N-phenylamino)ethylphenylborane is used as a reagent in the Suzuki-Miyaura coupling, a cross-coupling reaction between an organoboron compound and an organohalide or triflate, leading to the formation of new carbon-carbon bonds.
Used in the Stille Coupling:
(N-Methyl-N-phenylamino)ethylphenylborane is also used as a reagent in the Stille coupling, a cross-coupling reaction between an organotin compound and an organohalide or triflate, resulting in the formation of new carbon-carbon bonds.
Check Digit Verification of cas no
The CAS Registry Mumber 39967-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,6 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.Calculate Digit Verification of CAS Registry Number 39967-40:
(7*3)+(6*9)+(5*9)+(4*6)+(3*7)+(2*4)+(1*0)=173
173 % 10 = 3
So 39967-40-3 is a valid CAS Registry Number.
39967-40-3Upstream product
39967-40-3Downstream Products
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(N-Methyl-N-phenylamino)ethylphenylborane
