(R)-2-Chlorobutyric Acid
≥98%
- Product Code: 113526
CAS:
54053-45-1
| Molecular Weight: | 122.55 g./mol | Molecular Formula: | C₄H₇ClO₂ |
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| EC Number: | MDL Number: | MFCD00067098 | |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
(R)-2-Chlorobutyric Acid is primarily used in the synthesis of various pharmaceuticals and agrochemicals. It serves as a key chiral building block in the production of active pharmaceutical ingredients (APIs), particularly in the development of enantiomerically pure drugs. Its role is crucial in creating compounds with specific biological activities, such as anti-inflammatory or antimicrobial agents. Additionally, it is employed in organic synthesis to introduce chirality into molecules, which is essential for the efficacy and safety of many drugs. In agrochemicals, it is utilized to develop herbicides and pesticides with improved selectivity and lower environmental impact. Its application extends to research and development, where it is used as a reagent in asymmetric synthesis and stereochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | £41.93 |
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| 1.000 | 10-20 days | £121.93 |
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(R)-2-Chlorobutyric Acid
(R)-2-Chlorobutyric Acid is primarily used in the synthesis of various pharmaceuticals and agrochemicals. It serves as a key chiral building block in the production of active pharmaceutical ingredients (APIs), particularly in the development of enantiomerically pure drugs. Its role is crucial in creating compounds with specific biological activities, such as anti-inflammatory or antimicrobial agents. Additionally, it is employed in organic synthesis to introduce chirality into molecules, which is essential for the efficacy and safety of many drugs. In agrochemicals, it is utilized to develop herbicides and pesticides with improved selectivity and lower environmental impact. Its application extends to research and development, where it is used as a reagent in asymmetric synthesis and stereochemical studies.
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