(1S)-()-10-Camphorsulfonyl chloride
97%
- Product Code: 70816
Alias:
(1S)-(+)-camphor-10-sulfonyl chloride
CAS:
21286-54-4
| Molecular Weight: | 250.74 g./mol | Molecular Formula: | C₁₀H₁₅ClO₃S |
|---|---|---|---|
| EC Number: | 244-314-8 | MDL Number: | MFCD00064156 |
| Melting Point: | 67-68 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Used as a chiral derivatizing agent in the synthesis of enantiomerically pure compounds, particularly in the pharmaceutical industry for the separation and analysis of enantiomers. It is also employed in the preparation of sulfonamide derivatives, which are crucial intermediates in drug development. Additionally, it serves as a reagent in organic synthesis for the introduction of the camphorsulfonyl group, aiding in the study of stereochemistry and reaction mechanisms. Its application extends to the field of asymmetric catalysis, where it helps in creating chiral environments for selective chemical reactions.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 65 69? |
| PURITYTITRATION WITH AGNO3 | 96.5 103.5% |
| SPECIFIC ROTATION A20DC1CHCL3 | 31 34 |
| APPEARANCE | White to yellow powder |
| INFRARED SPECTRUM | Conforms to Structure |
| SOLUBILITY IN TOLUENE | almost transparency |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿320.00 |
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| 5.000 | 10-20 days | ฿830.00 |
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| 25.000 | 10-20 days | ฿3,390.00 |
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| 100.000 | 10-20 days | ฿11,990.00 |
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(1S)-()-10-Camphorsulfonyl chloride
Used as a chiral derivatizing agent in the synthesis of enantiomerically pure compounds, particularly in the pharmaceutical industry for the separation and analysis of enantiomers. It is also employed in the preparation of sulfonamide derivatives, which are crucial intermediates in drug development. Additionally, it serves as a reagent in organic synthesis for the introduction of the camphorsulfonyl group, aiding in the study of stereochemistry and reaction mechanisms. Its application extends to the field of asymmetric catalysis, where it helps in creating chiral environments for selective chemical reactions.
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