O-ethyl S-3-nitrobenzyl carbonodithioate
95 %
- Product Code: 53900
CAS:
1335107-28-2
Molecular Weight: | 257.3 g./mol | Molecular Formula: | C₁₀H₁₁NO₃S₂ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
O-ethyl S-3-nitrobenzyl carbonodithioate is primarily used in the field of organic synthesis as a reagent or intermediate. It plays a role in the preparation of various chemical compounds, particularly in the synthesis of heterocycles and other complex organic molecules. Its structure, featuring a nitrobenzyl group, makes it useful in reactions where nitro groups are required for further functionalization or transformation. Additionally, it can be employed in the development of agrochemicals and pharmaceuticals, where the nitrobenzyl moiety is often a key component in bioactive molecules. Its carbonodithioate group also allows it to participate in reactions involving sulfur-containing compounds, expanding its utility in synthetic chemistry.
Product Specification:
Test | Specification |
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Purity | 94.5 100% |
Appearance | Yellow solid |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿972.00 |
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1.000 | 10-20 days | ฿4,130.00 |
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5.000 | 10-20 days | ฿13,370.00 |
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O-ethyl S-3-nitrobenzyl carbonodithioate
O-ethyl S-3-nitrobenzyl carbonodithioate is primarily used in the field of organic synthesis as a reagent or intermediate. It plays a role in the preparation of various chemical compounds, particularly in the synthesis of heterocycles and other complex organic molecules. Its structure, featuring a nitrobenzyl group, makes it useful in reactions where nitro groups are required for further functionalization or transformation. Additionally, it can be employed in the development of agrochemicals and pharmaceuticals, where the nitrobenzyl moiety is often a key component in bioactive molecules. Its carbonodithioate group also allows it to participate in reactions involving sulfur-containing compounds, expanding its utility in synthetic chemistry.
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