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1-Oxoheptan-2-yl benzoate, also known as 2-oxoheptyl benzoate, is an organic compound with the chemical formula C14H18O3. It is a derivative of benzoic acid, where the hydrogen atom of the carboxyl group is replaced by a 2-oxoheptyl group. 1-oxoheptan-2-yl benzoate is characterized by its ester functional group, which is formed by the reaction of a carboxylic acid (benzoic acid) with an alcohol (2-oxoheptyl alcohol). 1-Oxoheptan-2-yl benzoate is a colorless to pale yellow liquid with a mild, fruity odor. It is used in the fragrance industry as a fixative and in the synthesis of other organic compounds. Due to its chemical structure, it is insoluble in water but soluble in organic solvents such as ethanol and ether.

59058-17-2

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59058-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59058-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,5 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59058-17:
(7*5)+(6*9)+(5*0)+(4*5)+(3*8)+(2*1)+(1*7)=142
142 % 10 = 2
So 59058-17-2 is a valid CAS Registry Number.

59058-17-2Relevant academic research and scientific papers

In situ generated (Hypo)iodite catalysts for the direct α-oxyacylation of carbonyl compounds with carboxylic acids

Uyanik, Muhammet,Suzuki, Daisuke,Yasui, Takeshi,Ishihara, Kazuaki

supporting information; experimental part, p. 5331 - 5334 (2011/07/08)

It′s the iodine: The intra- and intermolecular title reaction is catalyzed by an in situ generated ammonium (hypo)iodite species. Either H 2O2 or tert-butyl hydroperoxide (TBHP) can be used as an environmentally benign oxidant and a wide range of substrates react to give the corresponding α-acyloxycarbonyl compounds in good to excellent yields.

A general method for the α-acyloxylation of carbonyl compounds

Beshara, Cory S.,Hall, Adrian,Jenkins, Robert L.,Jones, Kerri L.,Jones, Teyrnon C.,Killeen, Niall M.,Taylor, Paul H.,Thomas, Stephen P.,Tomkinson, Nicholas C. O.

, p. 5729 - 5732 (2007/10/03)

(Chemical Equation Presented) A simple, one-pot method for the α-acyloxylation of carbonyl compounds that proceeds at room temperature in the presence of both moisture and air has been developed. Treatment of a variety of aldehydes and both cyclic and acy

The first synthesis of threo- and erythro-(E)-4,5-dihydroxydec-2-enals carbonyls related to the peroxidation of liver microsomal lipids

Allevi, Pietro,Cajone, Francesco,Ciuffreda, Pierangela,Anastasia, Mario

, p. 1347 - 1350 (2007/10/02)

The first synthesis of threo and erythro (E)-4,5-dihydroxydec-2-enals, aldehydes related to the lipid peroxidation is accomplished by reaction of α-benzoyloxheptanal with the Grignard reagent of 3,3-diethoxy-1-propyne and lithium aluminium hydride reducti

RESOLUTION AND DETERMINATION OF ENANTIOMERIC EXCESSES OF CHIRAL ALDEHYDES VIA CHIRAL IMIDAZOLIDINES

Mangeney, P.,Alexakis, A.,Normant, J. F.

, p. 2677 - 2680 (2007/10/02)

Enantiomeric purity of chiral aldehydes was determined by NMR analysis of derived imidazolidines.The diastereomeric imidazolidines were easily separated by silica gel column and converted into enantiomerically pure aldehyde by acid hydrolysis.

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