Allyl chloroformate

99%

  • Product Code: 135064
  CAS:    2937-50-0
Molecular Weight: 120.53 g./mol Molecular Formula: C₄H₅ClO₂
EC Number: MDL Number: MFCD00000648
Melting Point: Boiling Point:
Density: 1.134 g/mL at 20 °C(lit.) Storage Condition: 2~8℃
Product Description: Allyl chloroformate is primarily used as a reagent in organic synthesis, especially in the protection of functional groups such as amines and alcohols. It reacts readily to form allyl carbamate (alloc) and allyl carbonate derivatives, which are useful protecting groups in peptide and nucleotide synthesis due to their stability under a variety of reaction conditions and selective removal via palladium-catalyzed deprotection. It is also employed in the preparation of heterocyclic compounds and pharmaceutical intermediates. Its ability to introduce allyloxy carbonyl groups makes it valuable in the development of complex molecules in medicinal chemistry. Additionally, it serves as a building block in the synthesis of agrochemicals and specialty polymers. Due to its high reactivity and lachrymatory nature, it is handled with care in controlled environments, typically under inert atmosphere and with appropriate safety measures.
Product Specification:
Test Specification
Purity 98.5-100
Refractive Index (N20/D) 1.421-1.424
Appearance Clear liquid
Sizes / Availability / Pricing:
Size Availability Price Quantity
5g 10-20 days ฿330.00
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25g 10-20 days ฿580.00
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100g 10-20 days ฿1,380.00
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500g 10-20 days ฿4,990.00
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2.5kg 10-20 days ฿22,450.00
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Allyl chloroformate
Allyl chloroformate is primarily used as a reagent in organic synthesis, especially in the protection of functional groups such as amines and alcohols. It reacts readily to form allyl carbamate (alloc) and allyl carbonate derivatives, which are useful protecting groups in peptide and nucleotide synthesis due to their stability under a variety of reaction conditions and selective removal via palladium-catalyzed deprotection. It is also employed in the preparation of heterocyclic compounds and pharmaceutical intermediates. Its ability to introduce allyloxy carbonyl groups makes it valuable in the development of complex molecules in medicinal chemistry. Additionally, it serves as a building block in the synthesis of agrochemicals and specialty polymers. Due to its high reactivity and lachrymatory nature, it is handled with care in controlled environments, typically under inert atmosphere and with appropriate safety measures.
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