5-Benzyloxy-2-nitrotoluene
98%
- Product Code: 62861
Alias:
2-nitro-5-benzyloxy-toluene; 2-methyl-1-nitro-4-(phenylmethoxy)-;2-BENZYLOXY-2-NITROTOLUENE;5-BENZOXY-2-NITROTOLUENE;(3-Methyl-4 -nitrophenyl)benzyl ether
CAS:
22424-58-4
| Molecular Weight: | 243.26 g./mol | Molecular Formula: | C₁₄H₁₃NO₃ |
|---|---|---|---|
| EC Number: | 244-988-3 | MDL Number: | MFCD00024269 |
| Melting Point: | 69-70℃ | Boiling Point: | 400.3℃ at 760 mmHg |
| Density: | Storage Condition: | 2-8℃, dry, inert gas |
Product Description:
5-Benzyloxy-2-nitrotoluene is primarily used as an intermediate in organic synthesis, particularly in the production of dyes and pigments. Its structure allows it to participate in various chemical reactions, making it valuable for creating complex organic compounds. Additionally, it finds application in the development of pharmaceuticals, where it serves as a building block for synthesizing active pharmaceutical ingredients (APIs). The compound is also utilized in research laboratories for studying reaction mechanisms and developing new synthetic methodologies. Its nitro and benzyloxy groups make it a versatile reagent in the synthesis of aromatic compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | light yellow solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿610.00 |
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| 5.000 | 10-20 days | ฿2,110.00 |
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5-Benzyloxy-2-nitrotoluene
5-Benzyloxy-2-nitrotoluene is primarily used as an intermediate in organic synthesis, particularly in the production of dyes and pigments. Its structure allows it to participate in various chemical reactions, making it valuable for creating complex organic compounds. Additionally, it finds application in the development of pharmaceuticals, where it serves as a building block for synthesizing active pharmaceutical ingredients (APIs). The compound is also utilized in research laboratories for studying reaction mechanisms and developing new synthetic methodologies. Its nitro and benzyloxy groups make it a versatile reagent in the synthesis of aromatic compounds.
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