(1S)-(-)-Camphanic chloride
97%
- Product Code: 113050
Alias:
(-)-Bamphanyl chloride; (1S)-3-oxo-4,7,7-trimethyl-2-oxabicyclo[2.2.1]heptane-1-carbonyl chloride; (1S)-( -)-Bornane chloride; (-)-camphoric acid chloride; (+)-(1R,4S)-camphoryl chloride; (1S)-(-)-camphoric acid chloride
CAS:
39637-74-6
| Molecular Weight: | 216.66 g./mol | Molecular Formula: | C₁₀H₁₃ClO₃ |
|---|---|---|---|
| EC Number: | 254-552-4 | MDL Number: | MFCD00135626 |
| Melting Point: | 71-73 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
(1S)-(-)-Camphanic chloride is widely used in organic synthesis as a chiral derivatizing agent. It is particularly valuable in the resolution of racemic mixtures, enabling the separation of enantiomers for analytical and preparative purposes. This compound is also employed in the preparation of chiral auxiliaries and catalysts, which are crucial in asymmetric synthesis to produce enantiomerically pure compounds. Additionally, it finds application in the synthesis of biologically active molecules, such as pharmaceuticals, where stereochemistry plays a critical role in efficacy and safety. Its use extends to the modification of natural products and the creation of complex molecular architectures with defined stereochemistry.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Yellow To Orange-Brown Powder |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿450.00 |
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| 5.000 | 10-20 days | ฿2,020.00 |
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| 25.000 | 10-20 days | ฿9,490.00 |
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(1S)-(-)-Camphanic chloride
(1S)-(-)-Camphanic chloride is widely used in organic synthesis as a chiral derivatizing agent. It is particularly valuable in the resolution of racemic mixtures, enabling the separation of enantiomers for analytical and preparative purposes. This compound is also employed in the preparation of chiral auxiliaries and catalysts, which are crucial in asymmetric synthesis to produce enantiomerically pure compounds. Additionally, it finds application in the synthesis of biologically active molecules, such as pharmaceuticals, where stereochemistry plays a critical role in efficacy and safety. Its use extends to the modification of natural products and the creation of complex molecular architectures with defined stereochemistry.
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