58570-06-2

Basic information

• Product Name: 2-(benzoyloxy)-2-methylpropanoic acid chloride
• Synonyms: 2-(benzoyloxy)-2-methylpropanoic acid chloride
• CAS NO: 58570-06-2
• Molecular Weight: 226.66
• Mol File: 58570-06-2.mol

Chemical Properties

• CAS DataBase Reference: 2-(benzoyloxy)-2-methylpropanoic acid chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(benzoyloxy)-2-methylpropanoic acid chloride(58570-06-2)
• EPA Substance Registry System: 2-(benzoyloxy)-2-methylpropanoic acid chloride(58570-06-2)

Safety Data

• Hazardous Substances Data: 58570-06-2(Hazardous Substances Data)

Upstream product

• 58570-00-6 2-(benzoyloxy)-2-methylpropanoic acid 

Downstream Products

• 1379613-68-9 (2S)-2-amino-3-(3,4-bis((2-(benzoyloxy)-2-methylpropanoyl)oxy)phenyl)propanoic acid hydrochloride 
• 1379614-08-0 (2S)-2-amino-3-(3,4-bis((2-(benzoyloxy)-2-methylpropanoyl)oxy)phenyl)propanoic acid 
• 1379613-67-8 (2S)-3-((3,4-bis((2-benzoyloxy)-2-methylpropanoyl)oxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid 
• 1379614-09-1 (2S)-2-amino-3-(3,4-bis((2-(benzoyloxy)-2-methylpropanoyl)oxy)phenyl)propanoic acid tosylate 
• 1379613-66-7 (2S)-((4-(3-benzyloxy)-2-((tert-butoxycarbonyl)amino)-3-oxopropyl-1,2-phenylene)bis(oxy))bis(2-methyl-1-oxopropan-2,1-diyl)dibenzoate 
• 50896-85-0 (3aS)-3c-benzoyloxy-2t-hydroxymethyl-(3ar,9ac)-2,3,3a,9a-tetrahydro-furo[2',3':4,5]oxazolo[3,2-a]pyrimidin-6-ylideneamine 

Relevant articles and documents

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Metal-Free Photoinduced Hydroalkylation Cascade Enabled by an Electron-Donor-Acceptor Complex

A metal- A nd photocatalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a single electron transfer (SET) event involving a photoexcited electron-donor-acceptor complex between an NHPI ester and a Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. The method provides an operationally simple, robust, and step-economical approach toward the construction of diversely functionalized dihydroquinolinones bearing quaternary centers. A sequential one-pot hydroalkylation-isomerization approach is also offered, giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance were observed in both approaches.

NOVEL COMPOUND AND MEDICAL USE THEREOF

Provided is a levodopa prodrug that overcomes the problems attributed to the blood kinetics of levodopa such as large number of doses and the incidence of side effects due to frequent dosing. (2S)-2-Amino-3-(3,4-bis((2-(benzoyloxy)-2-methylpropanoyl)oxy)p