Cinnamoyl chloride
97%
- Product Code: 123088
Alias:
Cinnamoyl Chloride; 3-Phenyl-2-Acryloyl Chloride, 3-Phenyl Acryloyl Chloride
CAS:
102-92-1
Molecular Weight: | 166.6 g./mol | Molecular Formula: | C₉H₇ClO |
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EC Number: | 203-065-5 | MDL Number: | MFCD00000732 |
Melting Point: | 35-37 °C(lit.) | Boiling Point: | 256-258 °C(lit.) |
Density: | Storage Condition: | 2~8°C |
Product Description:
Used extensively in organic synthesis to introduce the cinnamoyl group into various compounds. It is a key intermediate in the production of pharmaceuticals, particularly for drugs targeting inflammation and microbial infections. In the fragrance and flavor industry, it is employed to create aromatic compounds with a cinnamon-like scent. Additionally, it serves as a building block in the synthesis of UV-absorbing materials for coatings and polymers. Its reactivity with amines and alcohols makes it valuable for producing esters and amides in research and industrial applications.
Product Specification:
Test | Specification |
---|---|
Melting Point | 33-37 |
Purity (GC) | 97-100 |
Appearance | White to yellow crystals, flakes, powder or solid |
Infrared Spectrum | Conforms To Structure |
Solubility in Dioxane | 0.1 g/mL, transparent solution |
Note | This product is a low melting point solid and may change state in different environments (solid, liquid, or semi-solid). |
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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500g | 10-20 days | ฿2,590.00 |
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2.5kg | 10-20 days | ฿12,700.00 |
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100g | 10-20 days | ฿820.00 |
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25g | 10-20 days | ฿320.00 |
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Cinnamoyl chloride
Used extensively in organic synthesis to introduce the cinnamoyl group into various compounds. It is a key intermediate in the production of pharmaceuticals, particularly for drugs targeting inflammation and microbial infections. In the fragrance and flavor industry, it is employed to create aromatic compounds with a cinnamon-like scent. Additionally, it serves as a building block in the synthesis of UV-absorbing materials for coatings and polymers. Its reactivity with amines and alcohols makes it valuable for producing esters and amides in research and industrial applications.
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