15784-26-6

Basic information

• Product Name: Propanoic acid, 2,2-dimethyl-, 2-propenyl ester
• Synonyms: Pivalinsaeureallylester;pivalic acid allyl ester;Propanoic acid,2,2-dimethyl-,2-propenyl ester;2-propenyl trimethylacetate;allyl pivaloate;allyl pivalate;allyl trimethylacetate;allyl dimethylpropionate
• CAS NO: 15784-26-6
• Molecular Formula: C8H14O2
• Molecular Weight: 142.198
• Mol File: 15784-26-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 55-56 °C(Press: 36 Torr)
• Density: 0.893±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Propanoic acid, 2,2-dimethyl-, 2-propenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 2,2-dimethyl-, 2-propenyl ester(15784-26-6)
• EPA Substance Registry System: Propanoic acid, 2,2-dimethyl-, 2-propenyl ester(15784-26-6)

Safety Data

• Hazardous Substances Data: 15784-26-6(Hazardous Substances Data)

Upstream product

• 1427308-57-3 C₁₀H₆F₆O₂S 
• 3282-30-2 pivaloyl chloride 
• 107-18-6 allyl alcohol 
• 80-62-6 methacrylic acid methyl ester 
• 765-30-0 Cyclopropylamine 
• 75-98-9 Trimethylacetic acid 

Downstream Products

• 1657-60-9 2,2-dimethyl-1,1-diphenyl-propan-1-ol 
• 1333-74-0 hydrogen 
• 189219-04-3 1-(2-allyl-4-methoxyphenyl)ethan-1-one 
• 14990-09-1 tert-butyl cinnamate 
• 114155-64-5 2-allylhydrocinnamic acid tert-butyl ester 
• 1855-63-6 cyclohex-1-enecarbonitrile 
• 4141-48-4 allyldiphenylphosphine oxide 
• 111464-55-2 (S)-(+)-2-methyl-2-phenyl-4-pentenylaldehyde 
• 67679-06-5 (R)-(-)-2-methyl-2-phenyl-4-pentenylaldehyde 

Relevant articles and documents

Generation and trapping of cyclopropyldiazonium and diazocyclopropane in the nitrosation of cyclopropylamine with alkyl nitrites

Diazocyclopropane and an cyclopropyldiazonium ion, which are highly reactive intermediates, can be generated and trapped by appropriate substrates immediately in the direct nitrosation of cyclopropylamine with alkyl nitrites. Diazocyclopropane is trapped

THE NITROGENATED ALLYLIC SYSTEM AS AN INTRAMOLECULAR NUCLEOPHILE: A NEW ROUTE TO PYRAZOLES

A new route to pyrazoles via the cyclization of N-allyl-N-nitrosoamides is described.