3,4-Dimethoxyphenyl Isothiocyanate
≥98%(GC)
- Product Code: 84484
CAS:
33904-04-0
Molecular Weight: | 195.24 g./mol | Molecular Formula: | C₉H₉NO₂S |
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EC Number: | MDL Number: | MFCD00041075 | |
Melting Point: | 48°C | Boiling Point: | |
Density: | Storage Condition: | Room temperature, dry, inert gas storage |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of various pharmacologically active molecules. It serves as a key intermediate in the preparation of heterocyclic compounds, which are often explored for their potential therapeutic properties, including anticancer, antimicrobial, and anti-inflammatory activities. Additionally, it is employed in the synthesis of specialized dyes and pigments due to its ability to introduce specific functional groups into complex structures. Its reactivity with amines and other nucleophiles makes it valuable in the creation of thiourea derivatives, which are studied for their biological and chemical applications.
Product Specification:
Test | Specification |
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APPEARANCE | White to Almost white powder to crystal |
PURITYGC | 98 100% |
MELTING POINT | 46.0-50.0 |
Infrared spectrum | Conforms to Structure |
NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $69.77 |
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5.000 | 10-20 days | $202.25 |
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25.000 | 10-20 days | $784.90 |
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3,4-Dimethoxyphenyl Isothiocyanate
This compound is primarily utilized in organic synthesis as a versatile building block for the development of various pharmacologically active molecules. It serves as a key intermediate in the preparation of heterocyclic compounds, which are often explored for their potential therapeutic properties, including anticancer, antimicrobial, and anti-inflammatory activities. Additionally, it is employed in the synthesis of specialized dyes and pigments due to its ability to introduce specific functional groups into complex structures. Its reactivity with amines and other nucleophiles makes it valuable in the creation of thiourea derivatives, which are studied for their biological and chemical applications.
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