Allyl 2,2,2-trichloroacetimidate

98%

  • Product Code: 83164
  CAS:    51479-73-3
Molecular Weight: 202.46 g./mol Molecular Formula: C₅H₆Cl₃NO
EC Number: MDL Number: MFCD00190710
Melting Point: Boiling Point: 145.5°C
Density: 1.36g/mL Storage Condition: room temperature, dry
Product Description: This chemical is primarily utilized in organic synthesis as a versatile reagent for the introduction of the allyl group into various molecules. It is particularly effective in glycosylation reactions, where it facilitates the formation of glycosidic bonds, a critical step in the synthesis of complex carbohydrates and glycoconjugates. The compound is also employed in the preparation of allyl ethers and esters, which are valuable intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to act as a protective group for alcohols and amines further enhances its utility in multi-step synthetic processes. Additionally, it is used in the development of polymeric materials and coatings, where it contributes to the modification of surface properties and the enhancement of material performance.
Product Specification:
Test Specification
APPEARANCE Colorless to Yellow Liquid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
REFRACTIVE INDEX N20D 1.483-1.487
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿1,480.00
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-
5.000 10-20 days ฿5,860.00
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-
25.000 10-20 days ฿19,900.00
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-
Allyl 2,2,2-trichloroacetimidate
This chemical is primarily utilized in organic synthesis as a versatile reagent for the introduction of the allyl group into various molecules. It is particularly effective in glycosylation reactions, where it facilitates the formation of glycosidic bonds, a critical step in the synthesis of complex carbohydrates and glycoconjugates. The compound is also employed in the preparation of allyl ethers and esters, which are valuable intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to act as a protective group for alcohols and amines further enhances its utility in multi-step synthetic processes. Additionally, it is used in the development of polymeric materials and coatings, where it contributes to the modification of surface properties and the enhancement of material performance.
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