16010-88-1

Basic information

• Product Name: tert-butyl 2-(4-hydroxyphenyl)acetate
• Synonyms: tert-butyl 2-(4-hydroxyphenyl)acetate
• CAS NO: 16010-88-1
• Molecular Weight: 208.257
• Mol File: 16010-88-1.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: tert-butyl 2-(4-hydroxyphenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 2-(4-hydroxyphenyl)acetate(16010-88-1)
• EPA Substance Registry System: tert-butyl 2-(4-hydroxyphenyl)acetate(16010-88-1)

Safety Data

• Hazardous Substances Data: 16010-88-1(Hazardous Substances Data)

Upstream product

• 156-38-7 4-hydroxyphenylacetate 
• 75-65-0 tert-butyl alcohol 
• 106-41-2 4-bromo-phenol 
• 51656-70-3 (2-tert-butoxy-2-oxoethyl)zinc(II) bromide 
• 7664-93-9 sulfuric acid 
• 115-11-7 isobutene 
• 2491-38-5 2-bromo-1-(4'-hydroxyphenyl)-1-ethanone 
• 188119-50-8 diethyl (2-(4-hydroxyphenyl)-2-oxoethyl) phosphate 
• 19712-89-1 tert-butyl 2-(4-benzyloxyphenyl)acetate 
• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 1694-31-1 tert-butyl acetoacetate 
• 36805-97-7 N,N-dimethylformamide di-tert-butyl acetal 
• 6547-53-1 2-[4-(benzyloxy)benzyl]acetic acid 
• 99-93-4 4-Hydroxyacetophenone 

Downstream Products

• 142935-27-1 3,3-diethyl-4-<<4-<<(1,1-dimethylethoxy)carbonyl>methyl>phenyl>oxy>-2-azetidinone 
• 16010-89-2 3-<4-Carboxy-methyl-phenoxy>-4-methoxy-phenylessigsaeure-methylester 
• 147055-86-5 [4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid 
• 1027034-44-1 [4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid tert-butyl ester 
• 345964-12-7 8,8-dimethyl-5-oxo-5,6,7,8-tetrahydro-naphthalene-2-carboxylic acid 4-(tert-butoxycarbonylmethyl)phenyl ester 
• 1241507-68-5 C₂₁H₂₅N₃O₃ 
• 1408065-23-5 C₃₆H₅₁N₃O₆ 
• 1408065-24-6 C₃₆H₅₃N₃O₄ 
• 1408065-25-7 C₃₇H₅₂N₄O₄ 
• 1408065-26-8 C₃₃H₄₄N₄O₄ 
• 1408065-22-4 C₁₉H₁₉NO₆ 
• 1620332-75-3 tert-butyl 4-[(10-bromodecyl)oxy]phenylcarbamate 
• 1620332-80-0 tert-butyl 4-[(10-{[4'-(decyloxy)-1,1'-biphenyl-4-yl]oxy}decyl)oxy]phenylcarbamate 
• 1620332-81-1 tert-butyl 4-({10-[(4'-cyano-1,1'-biphenyl-4-yl)oxy]decyl}oxy)phenylcarbamate 

Relevant articles and documents

Photoinduced Vitamin B12-Catalysis for Deprotection of (Allyloxy)arenes

Vitamin B12 is a natural cobalt complex that, while reduced to the "supernucleophilic" Co(I) form, can easily react with electrophiles via an SN2 mechanism. It is also shown to react via an SN2′ mechanism with allylic compounds allowing for photochemical deprotection of (allyloxy)arenes. A sustainable alternative to commonly used noble metal-catalyzed deprotection reactions is presented.

Optimisation of BACE1 inhibition of tripartite structures by modification of membrane anchors, spacers and pharmacophores - Development of potential agents for the treatment of Alzheimer's disease

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