2-aminobutanenitrile hydrochloride
95%
- Product Code: 61804
CAS:
93554-80-4
Molecular Weight: | 84.12 g./mol | Molecular Formula: | C₄H₃N₂HCl |
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EC Number: | MDL Number: | MFCD11858092 | |
Melting Point: | 144-146 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. It is particularly valuable in the synthesis of active pharmaceutical ingredients (APIs) that target neurological conditions, such as anticonvulsants or antidepressants. Its nitrile group allows for further functionalization, making it versatile in creating complex molecules. Additionally, it is employed in the development of agrochemicals, including herbicides and pesticides, due to its ability to introduce specific functional groups into target structures. In research, it is utilized to study reaction mechanisms and develop novel synthetic pathways.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | solid |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
PURITY NMR | 94.5 100% |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.025 | 10-20 days | ฿2,700.00 |
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0.050 | 10-20 days | ฿5,000.00 |
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0.250 | 10-20 days | ฿19,650.00 |
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1.000 | 10-20 days | ฿39,410.00 |
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2-aminobutanenitrile hydrochloride
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. It is particularly valuable in the synthesis of active pharmaceutical ingredients (APIs) that target neurological conditions, such as anticonvulsants or antidepressants. Its nitrile group allows for further functionalization, making it versatile in creating complex molecules. Additionally, it is employed in the development of agrochemicals, including herbicides and pesticides, due to its ability to introduce specific functional groups into target structures. In research, it is utilized to study reaction mechanisms and develop novel synthetic pathways.
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