614-44-8

Basic information

• Product Name: Acetic acid, (benzoyloxy)-
• CAS NO: 614-44-8
• Molecular Formula: C9H8O4
• Molecular Weight: 180.16
• Mol File: 614-44-8.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Acetic acid, (benzoyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, (benzoyloxy)-(614-44-8)
• EPA Substance Registry System: Acetic acid, (benzoyloxy)-(614-44-8)

Safety Data

• Hazardous Substances Data: 614-44-8(Hazardous Substances Data)

Upstream product

• 94-33-7 C₉H₁₀O₃ 
• 29747-05-5 methyl O^α-benzoylglycolate 
• 98-88-4 benzoyl chloride 
• 939-56-0 benzoyloxyacetonitrile 
• 20847-03-4 O¹,O⁶-dibenzoyl-galactitol 
• 532-32-1 sodium benzoate 
• 65-85-0 benzoic acid 
• 936-51-6 2-phenyl-1,3-dioxolane 
• 56-23-5 tetrachloromethane 
• 54339-95-6 1,4-bis-benzoyloxy-but-2-yne 
• 10028-15-6 ozone 
• 64-19-7 acetic acid 
• 495-69-2 Hippuric Acid 
• 7697-37-2 nitric acid 

Downstream Products

• 54150-57-1 2-benzoyloxyacetyl chloride 
• 79-14-1 glycolic Acid 
• 65-85-0 benzoic acid 
• 93-58-3 benzoic acid methyl ester 
• 50-00-0 formaldehyd 
• 54354-04-0 benzoic acid methoxymethyl ester 
• 29747-05-5 methyl O^α-benzoylglycolate 
• 1341219-68-8 O-benzoyl-N-(4-tert-butyldimethylsiloxy-2-methoxybenzyl)-N-(4-methoxyphenyl)glycolamide 
• 115178-81-9 Benzoic acid [(2-dimethylamino-ethyl)-methyl-carbamoyl]-methyl ester 
• 106231-69-0 Benzoic acid 2-((S)-2-carbamoyl-pyrrolidin-1-yl)-2-oxo-ethyl ester 
• 106231-70-3 Benzoic acid 2-(4-methyl-piperazin-1-yl)-2-oxo-ethyl ester 
• 106231-54-3 2-(dimethylamino)-2-oxoethyl benzoate 
• 64649-57-6 O-Benzoyl-N-ethylglycolsaeureamid 
• 64649-43-0 (aminocarbonyl)methyl benzoate 

Relevant articles and documents

Domino Two-Step Oxidation of β-Alkoxy Alcohols to Hemiacetal Esters: Linking a Stoichiometric Step to an Organocatalytic Step with a Common Organic Oxidant

Primary and secondary β-alkoxy alcohols can be cleanly and efficiently oxidized into hemiacetal esters in a cascade two-step process. mCPBA serves both as a stoichiometric oxidant in the first TEMPO-catalyzed step, converting alcohols to aldehydes/ketones, and as a reagent in the second Baeyer–Villiger stoichiometric oxidation, transforming the aldehydes/ketones into hemiacetal esters. The use of an oxidant common to both steps enables the domino reaction to proceed under a single experimental setting. Longer oxidative cascade sequences are possible when this new methodology is applied to suitable substrates.

IMIDAZO(1,2-a)PYRIDINE DERIVATIVE

A compound reprsented by the following formula (I), its salts or nsolvates thereof capable of specifically or selectively expressig an antifungal activity in a broad spectrum based on the novel mechanism thereof of 1,6-β-glucan synthesis inhibition, and an antifungal agent containing any of them.

The Effect of pH Control on the Selective Ruthenium-Catalyzed Oxidation of Ethers and Alcohols with Sodium Hypochlorite

Highly selective oxidations of ethers to esters or lactones and of secondary alcohols to ketones were achieved using catalytic amounts of various Ru precursors and the theoretical amount of NaOCl. Reactions were carried out in biphasic solvent mixtures at constant pH 9-9.5 via either feed-on-demand addition of HCl and NaOH or in the presence of NaHCO3/Na 2CO3 buffer. The catalyst could be easily recycled for at least 4 times with only minor loss in selectivity. Products were generally recovered by simple phase separation and evaporation of the organic solvent. The effects of catalyst precursor, additives and pH control method are also described.