19444-23-6

Basic information

• Product Name: Benzyl 2-Hydroxy-2-Methylpropionate
• Synonyms: Benzyl 2-Hydroxy-2-Methylpropionate;Benzyl 2-hydroxy-2-methylpropanoate
• CAS NO: 19444-23-6
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.22706
• Mol File: 19444-23-6.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Benzyl 2-Hydroxy-2-Methylpropionate(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl 2-Hydroxy-2-Methylpropionate(19444-23-6)
• EPA Substance Registry System: Benzyl 2-Hydroxy-2-Methylpropionate(19444-23-6)

Safety Data

• Hazardous Substances Data: 19444-23-6(Hazardous Substances Data)

Usage

Uses

Benzyl 2-Hydroxy-2-methylpropionate is a useful chemical in organic synthesis.

Upstream product

• 594-61-6 2-methyllactic acid 
• 100-51-6 benzyl alcohol 
• 993-48-6 α-Hydroxy-2-methylpropionic acid Na salt 
• 100-44-7 benzyl chloride 
• 13027-88-8 2-hydroxyisobutyramide 
• 7285-83-8 2,4,6-tris(benzyloxy)-1,3,5-triazine 
• 7051-34-5 cyclopropylcarbinyl bromide 
• 100-39-0 benzyl bromide 
• 2495-37-6 benzyl methacrylate 

Downstream Products

• 1428848-57-0 1-(benzyloxy)-2-methyl-1-oxopropan-2-yl 4-(N-(tert-butoxycarbonyl)methylsulfonamido)-3-(cyclopropylmethoxy)benzoate 
• 1370712-57-4 C₁₈H₂₀O₃ 
• 1370712-58-5 benzyl 2-methyl-2-(3-methylphenoxy)propionate 
• 1370712-56-3 C₁₇H₁₈O₃ 
• 1370712-59-6 C₁₈H₂₀O₃ 
• 1370712-63-2 C₂₀H₂₄O₅ 
• 1370712-62-1 C₁₉H₂₂O₅ 
• 1370712-61-0 benzyl 2-[3-(methoxymethoxy)phenoxy]-2-methylpropanoate 
• 1370712-60-9 C₁₉H₂₂O₅ 
• 1159999-13-9 benzyl 2-[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoate 
• 77140-20-6 5,5-dimethyl-4-benzyloxy-[5H]furan-2-one 
• 1000296-72-9 α-ethoxy-isobutyric acid benzyl ester 
• 2495-37-6 benzyl methacrylate 

Relevant articles and documents

Synthesis and Applications of Unquaternized C-Bound Boron Enolates

A general and facile method to prepare unquaternized C-bound boron enolates by a ligand-controlled O-to-C isomerization is reported. Using this protocol, C-bound pinacolboron enolates have been isolated in pure form for the first time, and have been fully characterized by NMR spectroscopy and X-ray crystallography. In contrast to the general perception, such C-boron enolates are stable without coordinative saturation at the boron. Moreover, C-boron enolates present reactivities that are distinct from the O-boron enolates, and their applications in C-O and C-C bond formations are demonstrated.

Versatile and sustainable alcoholysis of amides by a reusable CeO 2 catalyst

CeO2 catalyzed the esterification between an equivalent molar ratio of primary amides and alcohols under neutral conditions, which provides the first versatile reusable catalytic system for direct alcoholysis of amides to esters with wider scope and 67 times higher turnover number (TON) than previous catalytic systems.

DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS

The invention relates to inhibitors of the phosphodiesterase 4 (PDE4) enzyme. More particularly, the invention relates to compounds that are derivatives of 1-phenyl-2-pyridinyl alkyl alcohols, methods of preparing such compounds, compositions containing them and therapeutic use thereof.