117048-44-9

Basic information

• Product Name: Acetic acid, [4-(hydroxymethyl)phenoxy]-, methyl ester
• CAS NO: 117048-44-9
• Molecular Formula: C10H12O4
• Molecular Weight: 196.203
• Mol File: 117048-44-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Acetic acid, [4-(hydroxymethyl)phenoxy]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, [4-(hydroxymethyl)phenoxy]-, methyl ester(117048-44-9)
• EPA Substance Registry System: Acetic acid, [4-(hydroxymethyl)phenoxy]-, methyl ester(117048-44-9)

Safety Data

• Hazardous Substances Data: 117048-44-9(Hazardous Substances Data)

Upstream product

• 623-05-2 (4-hydroxyphenyl)methanol 
• 96-32-2 bromoacetic acid methyl ester 
• 73620-18-5 methyl (4-formylphenoxy)acetate 
• 68858-21-9 [4-(hydroxymethyl)phenoxy]acetic acid 
• 74-88-4 methyl iodide 
• 96-34-4 methyl chloroacetate 

Downstream Products

• 551772-78-2 (4-{10-[10-(4-methoxycarbonylmethoxy-benzyloxycarbonylamino)-decyldisulfanyl]-decylcarbamoyloxymethyl}-phenoxy)-acetic acid methyl ester 
• 936257-15-7 (4-Acetoxymethyl-phenoxy)-acetic Acid Methyl Ester 
• 1566585-88-3 C₁₉H₂₈N₂O₆ 
• 1566585-83-8 C₂₆H₃₁N₃O₁₀ 
• 1566585-86-1 C₁₅H₂₄N₂O₅ 
• 913078-95-2 methyl (4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenoxy)acetate 
• 834914-27-1 {4-[6-(2-dimethylamino-propionyl)-naphthalen-2-yloxymethyl]-phenoxy}-acetic acid methyl ester 
• 104508-23-8 methyl 2-(4-(bromomethyl)phenoxy)acetate 

Relevant articles and documents

BENZENE FUSED HETEROCYCLIC DERIVATIVE AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

The present disclosure provides a benzene fused heterocyclic derivative of Formula (I): --?-?-? is a single or double bond; n is an integer of 0 or 1; A is -CH2-, -CH(OH)-, or - C(O)-; G is C or N; X is -CH2-, O, or -C(O)-; Y is alky

FUNCTIONALIZED PHENOLIC COMPOUNDS AND POLYMERS THEREFROM

The present invention relates to compounds of formula I, which are functionalized phenolic compounds, and polymers formed from the same. Ar—[O—(X)p—R′]q??I Polymers formed from the functionalized phenolics are expected to have controllable degradation profiles, enabling them to release an active component over a desired time range. The polymers are also expected to be useful in a variety of medical applications.

Surfaces designed for charge reversal

We have created surfaces which switch from cationic at pH 5, by attaching aminodicarboxylic acid units to silica and gold substrates. Charge reversal was demonstrated by monitoring the adsorption of cationic dyes (methylene blue and