(R)-1-amino-3-methylbutylboronic acid is an organoboronic acid derivative that is utilized in organic synthesis and pharmaceutical research. It is characterized by a boron atom attached to a 1-amino-3-methylbutyl group, which allows it to form stable boronate complexes with diols or polyols. These complexes are particularly useful in Suzuki-Miyaura cross-coupling reactions, a method for forming carbon-carbon bonds, making (R)-1-aMino-3-Methylbutylboronic acid a valuable asset in the construction of complex organic molecules. Furthermore, (R)-1-amino-3-methylbutylboronic acid holds potential in the development of new drugs and pharmaceuticals.
389799-97-7
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Basic information
- Product Name: (R)-1-aMino-3-Methylbutylboronic acid
- Synonyms: (R)-1-aMino-3-Methylbutylboronic acid
- CAS NO:389799-97-7
- Molecular Formula: C5H14BNO2
- Molecular Weight: 130.98116
- EINECS: N/A
- Product Categories: N/A
- Mol File: 389799-97-7.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 238.0±42.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 0.988±0.06 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 8.96±0.43(Predicted)
- CAS DataBase Reference: (R)-1-aMino-3-Methylbutylboronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (R)-1-aMino-3-Methylbutylboronic acid(389799-97-7)
- EPA Substance Registry System: (R)-1-aMino-3-Methylbutylboronic acid(389799-97-7)
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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: 389799-97-7(Hazardous Substances Data)
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389799-97-7 Usage
Uses
Used in Pharmaceutical Research:(R)-1-amino-3-methylbutylboronic acid is used as a key intermediate in the synthesis of various pharmaceuticals and bioactive molecules. Its ability to form stable boronate complexes with diols or polyols makes it a crucial component in the development of new drugs and pharmaceuticals.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-1-amino-3-methylbutylboronic acid is used as a reagent for the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. This application is significant in the construction of complex organic molecules, which are essential in the creation of novel compounds with potential applications in various industries.
Used in Drug Development:
(R)-1-amino-3-methylbutylboronic acid is also utilized in the development of new drugs, thanks to its potential to enhance the properties of pharmaceutical compounds. Its role in forming stable boronate complexes can lead to the creation of more effective and targeted therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 389799-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,7,9 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.Calculate Digit Verification of CAS Registry Number 389799-97:
(8*3)+(7*8)+(6*9)+(5*7)+(4*9)+(3*9)+(2*9)+(1*7)=257
257 % 10 = 7
So 389799-97-7 is a valid CAS Registry Number.
389799-97-7Upstream product
389799-97-7Downstream Products
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(R)-1-aMino-3-Methylbutylboronic acid
