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Sigma Aldrich Chloromethyl pivalate

Catalog No. 14118625G Shop All MilliporeSigma Sigma Organic Chemistry Products
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14-118-625G 25 g
14-118-6100G 100 g
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Description

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

  • Chloromethyl pivalate reacts with sodium salt of sulbactam to yield sulbactam pivoxil
  • It undergoes acylation reaction with 9-(2-phosphonylmethoxyethyl)adenine (pmea) to yield bis(pivaloyloxymethyl) pmea.chloromethyl pivalate was used in the synthesis of pivaloyloxy methyl ester of ofloxacin as prodrug
  • It was used as the reagent during the synthesis of an isoindoline-annulated, tricyclic sultam library via microwave-assisted, continuous-flow organic synthesis

Specifications

CAS 18997-19-8
Density 1.045 g/mL (at 25°C (literature))
Boiling Point 146°C to 148°C (lit.)
Molecular Formula C6H11ClO2
Linear Formula (CH3)3 CCOOCH2Cl
Refractive Index n20/D 1.417 (literature)
MDL Number MFCD00000884
Quantity 25 g
Synonym POM-Cl; Pivaloyloxymethyl chloride
Molecular Weight (g/mol) 150.6
Percent Purity 97%
Biological Activity Respiratory System
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