7481-22-3Relevant articles and documents
The reaction of o-(bromomethyl)benzeneboronic anhydride with primary amines.
Hawkins,Blackham
, p. 597 - 600 (2007/10/05)
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7481-22-3
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Basic information
- Product Name: [2-(tert-butylamino-methyl)-phenyl]-boronic acid
- Synonyms:
- CAS NO:7481-22-3
- Molecular Formula:
- Molecular Weight: 207.08
- EINECS: N/A
- Product Categories: N/A
- Mol File: 7481-22-3.mol
- Article Data: 1
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: [2-(tert-butylamino-methyl)-phenyl]-boronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: [2-(tert-butylamino-methyl)-phenyl]-boronic acid(7481-22-3)
- EPA Substance Registry System: [2-(tert-butylamino-methyl)-phenyl]-boronic acid(7481-22-3)
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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: 7481-22-3(Hazardous Substances Data)
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7481-22-3 Usage
Description
[2-(tert-butylamino-methyl)-phenyl]-boronic acid is a boronic acid derivative featuring a bulky tert-butylamino-methyl group attached to the phenyl ring. [2-(tert-butylamino-methyl)-phenyl]-boronic acid is known for its unique properties and reactivity, making it a valuable tool in organic chemistry.Uses
Used in Organic Synthesis:[2-(tert-butylamino-methyl)-phenyl]-boronic acid is used as a reagent in various organic synthesis reactions due to its steric hindrance provided by the tert-butylamino-methyl group, which influences the reactivity and selectivity of the compound.
Used in Metal-Catalyzed Cross-Coupling Reactions:
[2-(tert-butylamino-methyl)-phenyl]-boronic acid serves as a versatile ligand in metal-catalyzed cross-coupling reactions, further enhancing its utility in organic chemistry.
Used in Pharmaceutical Development:
[2-(tert-butylamino-methyl)-phenyl]-boronic acid is used as a building block or intermediate in the development of pharmaceuticals, leveraging its unique properties and reactivity.
Used in Agrochemicals:
[2-(tert-butylamino-methyl)-phenyl]-boronic acid is also utilized in the development of agrochemicals, where its specific reactivity and properties can be advantageous.
Used in Materials Science:
[2-(tert-butylamino-methyl)-phenyl]-boronic acid finds applications in materials science, where its properties can contribute to the creation of novel materials with desired characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 7481-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,8 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.Calculate Digit Verification of CAS Registry Number 7481-22:
(6*7)+(5*4)+(4*8)+(3*1)+(2*2)+(1*2)=103
103 % 10 = 3
So 7481-22-3 is a valid CAS Registry Number.
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[2-(tert-butylamino-methyl)-phenyl]-boronic acid
