17833-56-6

Basic information

• Product Name: Methyl 4-(methoxymethyl)phenylacetate
• Synonyms: Methyl 4-(methoxymethyl)phenylacetate;2-(4-(2-Methoxy-2-oxoethyl)phenyl)acetic acid
• CAS NO: 17833-56-6
• Molecular Formula: C₁₁H₁₂O₄
• Molecular Weight: 194
• Mol File: 17833-56-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl 4-(methoxymethyl)phenylacetate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 4-(methoxymethyl)phenylacetate(17833-56-6)
• EPA Substance Registry System: Methyl 4-(methoxymethyl)phenylacetate(17833-56-6)

Safety Data

• Hazardous Substances Data: 17833-56-6(Hazardous Substances Data)

Upstream product

• 622-75-3 1,4-phenylenediacetonitrile 
• 7325-46-4 1,4-phenylenediacetic acid 
• 36076-25-2 (4-methoxycarbonylmethylphenyl)acetic acid methyl ester 

Downstream Products

• 4253-33-2 bibenzyl-4,4'-diyl-di-acetic acid dimethyl ester 
• 115414-80-7 (4-Methoxymethyl-phenyl)-acetic acid methyl ester 
• 120167-84-2 bis (N-dodecyl acetamido)-1,4 butane 
• 282088-96-4 4-[[[4-[[[4-[[p-(methoxycarbonyl)phenylenecarbonyl]amino]-1-methyl-2-pyrrolyl]carbonyl]amino]-1-methyl-2-pyrrolyl]carbonyl]amino]-1-methyl-N-[3-(N,N-dimethylamino)propyl]-2-pyrrolecarboxamide 
• 191871-32-6 [4-(tert-butoxycarbonylamino-methyl)-phenyl]-acetic acid methyl ester 
• 1251957-87-5 2-[4-(2-{[(2R)-2-hydroxy-2-(pyridin-3-yl)ethyl]amino}-2-methylpropyl)phenyl]-N-(5-methylisoxazol-3-yl)acetamide 
• 1251957-82-0 2-[4-(2-hydroxy-2-methylpropyl)phenyl]-N-(5-methylisoxazol-3-yl)acetamide 
• 1251957-84-2 2-[4-(2-amino-2-methylpropyl)phenyl]-N-(5-methylisoxazol-3-yl)acetamide 
• 1251957-86-4 2-[4-(2-{[(2R)-2-(6-chloropyridin-3-yl)-2-hydroxyethyl]amino}-2-methylpropyl)phenyl]-N-(5-methylisoxazol-3-yl)acetamide 
• 861448-74-0 [4-(2-hydroxy-2-methylpropyl)phenyl]acetic acid 
• 129506-80-5 methyl 2-[4-(2-hydroxyethyl)phenyl]acetate 
• 96524-70-8 methyl 2-(4-formylphenyl)acetate 

Relevant articles and documents

Cyclic tris-[5]helicenes with single and triple twisted M?bius topologies and M?bius aromaticity

A number of singly (180°) twisted, largely single-stranded and thus conformationally rather fragile, M?bius molecules have been synthesized within the last 15 years, which are aromatic with 4n electrons, thus violating the Hückel rule. Annulenes with sign

Application of biocatalysis towards asymmetric reduction and hydrolytic desymmetrisation in the synthesis of a β-3 receptor agonist

Chemoenzymatic syntheses of two key intermediates in the preparation of a potent β-3 receptor agonist 1 are described. A lipase-catalysed hydrolytic desymmetrisation is employed in a new synthesis of intermediate 7, which avoids the use of alkyl-tin reagents. A second biotransformation delivers chiral chlorohydrin 5 from its parent ketone in greater enantiomeric excess than the previously-described Noyori-reduction process. A brief discussion of the enantioselectivity of a set of single-point mutants of Sporobolomyces salmonicolor aldehyde reductase in this bioreduction is also presented.