m-Toluoyl chloride
98%
- Product Code: 123336
Alias:
m-methylbenzoyl chloride; 3-methylbenzoyl chloride
CAS:
1711-06-4
Molecular Weight: | 154.59 g./mol | Molecular Formula: | C₈H₇ClO |
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EC Number: | 216-976-8 | MDL Number: | MFCD00000681 |
Melting Point: | -23°C | Boiling Point: | 86 °C (5 mmHg) |
Density: | 1.17 | Storage Condition: | room temperature, dry |
Product Description:
m-Toluoyl chloride is widely used as a key reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. It serves as an acylating agent, enabling the introduction of the m-toluoyl group into target molecules, which is crucial for the development of active pharmaceutical ingredients (APIs). Additionally, it is employed in the production of dyes, pigments, and fragrances, where it acts as an intermediate in the synthesis of complex organic compounds. Its reactivity with alcohols and amines makes it valuable in creating esters and amides, which are foundational structures in many industrial and research applications.
Product Specification:
Test | Specification |
---|---|
Purity (GC) | 97.5-100 |
Refractive Index N20/D | 1.548-1.55 |
Specific Gravity (20/20) | 1.171-1.174 |
Appearance | Colorless To Pale Brown Liquid |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿290.00 |
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25.000 | 10-20 days | ฿340.00 |
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100.000 | 10-20 days | ฿800.00 |
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500.000 | 10-20 days | ฿2,790.00 |
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2500.000 | 10-20 days | ฿12,300.00 |
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m-Toluoyl chloride
m-Toluoyl chloride is widely used as a key reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. It serves as an acylating agent, enabling the introduction of the m-toluoyl group into target molecules, which is crucial for the development of active pharmaceutical ingredients (APIs). Additionally, it is employed in the production of dyes, pigments, and fragrances, where it acts as an intermediate in the synthesis of complex organic compounds. Its reactivity with alcohols and amines makes it valuable in creating esters and amides, which are foundational structures in many industrial and research applications.
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