()-10,2-Camphorsultam
97%
- Product Code: 62491
Alias:
(1R,2S)-(+)-2,10-camphorylidene sulfonamide
CAS:
108448-77-7
Molecular Weight: | 215.31 g./mol | Molecular Formula: | C₁₀H₁₇NO₂S |
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EC Number: | MDL Number: | MFCD00151762 | |
Melting Point: | 185-187 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. It is effective in controlling stereochemistry during reactions like aldol additions, Diels-Alder reactions, and alkylations. Its rigid structure and ability to induce high enantioselectivity make it valuable in pharmaceutical and fine chemical industries for producing chiral intermediates. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, enhancing the efficiency and selectivity of synthetic routes.
Product Specification:
Test | Specification |
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Melting point | 182-186 |
PurityGC | 97-100 |
SPECIFIC ROTATION A20DC1CHCL3 | 30-35 |
APPEARANCE | White to off-white powder,crystals and/or chunks |
INFRARED SPECTRUM | Conforms to Structure |
SOLUBILITY IN CHLOROFORM | almost transparency |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿320.00 |
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5.000 | 10-20 days | ฿930.00 |
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25.000 | 10-20 days | ฿3,680.00 |
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100.000 | 10-20 days | ฿14,600.00 |
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()-10,2-Camphorsultam
Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. It is effective in controlling stereochemistry during reactions like aldol additions, Diels-Alder reactions, and alkylations. Its rigid structure and ability to induce high enantioselectivity make it valuable in pharmaceutical and fine chemical industries for producing chiral intermediates. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, enhancing the efficiency and selectivity of synthetic routes.
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