52252-58-1

Basic information

• Product Name: 2-(4-Hydroxybenzyl)acetessigsaeure-ethylester
• Synonyms: 2-(4-Hydroxybenzyl)acetessigsaeure-ethylester
• CAS NO: 52252-58-1
• Molecular Weight: 236.268
• Mol File: 52252-58-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-(4-Hydroxybenzyl)acetessigsaeure-ethylester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-Hydroxybenzyl)acetessigsaeure-ethylester(52252-58-1)
• EPA Substance Registry System: 2-(4-Hydroxybenzyl)acetessigsaeure-ethylester(52252-58-1)

Safety Data

• Hazardous Substances Data: 52252-58-1(Hazardous Substances Data)

Upstream product

• 141-97-9 ethyl acetoacetate 
• 123-08-0 4-hydroxy-benzaldehyde 
• 36600-75-6 2-(4-methoxy-benzyl)-3-oxo-butyric acid ethyl ester 
• 24405-45-6 ethyl 2-(4-methoxybenzylidene)-3-oxobutanoate 
• 123-11-5 4-methoxy-benzaldehyde 
• 609-14-3 2-acetylpropanoic acid ethyl ester 
• 108-95-2 phenol 
• 58714-57-1 E-2-(4-Hydroxybenzyliden)acetessigsaeure-ethylester 
• 7440-02-0 nickel 
• 58714-57-1 Z-2-(4-Hydroxybenzyliden)acetessigsaeure-ethylester 
• 2937-64-6 4-(acetyloxy)benzyl acetate 

Downstream Products

• 75999-07-4 5-(4-Hydroxybenzyl)-2,4-dimethylpyrimidin-6-ol 
• 17187-55-2 5-(4-Hydroxybenzyl)-4-methylpyrimidin-2,6-diol 
• 75999-01-8 4-(4-Hydroxybenzyl)-3-methylpyrazol-5-ol 
• 75999-02-9 4-(4-Hydroxybenzyl)-1,3-dimethylpyrazol-5-ol 
• 75999-05-2 1-(3-Chlorphenyl)-4-(4-hydroxybenzyl)-3-methylpyrazol-5-ol 
• 75999-19-8 Methylcarbaminsaeure-<4-(5-hydroxy-1,3-dimethylpyrazol-4-ylmethyl)phenylester> 
• 75999-21-2 Dimethylcarbaminsaeure-<4-(4-hydroxybenzyl)-1,3-dimethylpyrazol-5-ylester> 
• 75999-18-7 Methylcarbaminsaeure-<4-(6-hydroxy-2,4-dimethylpyrimidin-5-ylmethyl)phenylester> 
• 75999-23-4 3-Methyl-2-butensaeure-<4-(4-hydroxybenzyl)-5-methyl-1-(3-methyl-2-butenoyl)pyrazol-3-ylester> 
• 75999-22-3 Thiophosphorsaeure-O,O-diethyl-O-<4-hydroxybenzyl-1,3-dimethylpyrazol-5-yl>ester 
• 75999-20-1 Methylcarbaminsaeure-<4-<1-(3-chlorphenyl)-5-hydroxy-3-methylpyrazol-4-ylmethyl>phenylester> 
• 75999-24-5 3-Methyl-2-butensaeure-<5-methyl-1-<3-methyl-2-butenoyl>-4-<4-(3-methyl-2-butenoyloxy)benzyl>pyrazol-3-ylester> 
• 1390630-45-1 C₁₃H₁₅BrO₄ 
• 109152-30-9 psammaplin A 

Relevant articles and documents

All-natural carbon source raspberry ketone preparation method

The invention discloses an all-natural carbon source raspberry ketone preparation method, which comprises: carrying out a demethylation reaction on naturally-derived p-anisaldehyde as a raw material to prepare p-hydroxybenzaldehyde, carrying out a Knoevenagel condensation reaction on the p-hydroxybenzaldehyde and ethyl acetoacetate derived from biomass to obtain ethyl (E/Z)-2-acetyl-3-(4-hydroxyphenyl)acrylate, and carrying out hydrogenation, hydrolysis and decarboxylation to prepare the raspberry ketone. According to the present invention, the method can achieve the preparation of the all-natural carbon source raspberry ketone, and has advantages of simple route, easy operation, environmental friendliness, high yield and the like.

Efficient synthetic method of Psammaplin A

A new concise and efficient synthetic method of Psammaplin A was developed. Psammaplin A was obtained with 50% overall yield in nine steps from p-hydroxybenzaldehyde and ethyl acetoacetate via Knoevenagel condensation and direct nitrosation as key steps.

Beta-ketoester compounds

The beta-ketoesters of formula I are useful as precursors for organoleptic compounds, especially for flavors, fragrances and masking agents and antimicrobial compounds.