2-Amino-5-methylnicotinonitrile
98%
- Product Code: 63339
CAS:
38076-78-7
| Molecular Weight: | 133.15 g./mol | Molecular Formula: | C₇H₇N₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07779068 | |
| Melting Point: | Boiling Point: | 310.56°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of compounds with potential therapeutic effects, particularly in the creation of molecules targeting neurological and metabolic disorders. Additionally, it is employed in organic synthesis to construct complex heterocyclic structures, which are often found in drugs with anti-inflammatory, antiviral, or anticancer properties. Its nitrile and amino functional groups make it a versatile building block for further chemical modifications, enabling the production of diverse biologically active molecules.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white powder or crystals |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | €44.32 |
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| 0.250 | 10-20 days | €134.02 |
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2-Amino-5-methylnicotinonitrile
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of compounds with potential therapeutic effects, particularly in the creation of molecules targeting neurological and metabolic disorders. Additionally, it is employed in organic synthesis to construct complex heterocyclic structures, which are often found in drugs with anti-inflammatory, antiviral, or anticancer properties. Its nitrile and amino functional groups make it a versatile building block for further chemical modifications, enabling the production of diverse biologically active molecules.
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