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3-Cyclohexylpropyl 2-phenylacetate is a chemical compound with the molecular formula C18H24O2. It is an ester derived from cyclohexane and phenylacetic acid, featuring a cyclohexylpropyl group attached to the ester functional group. 3-cyclohexylpropyl 2-phenylacetate is characterized by its unique structure, which combines the cyclic nature of cyclohexane with the aromatic properties of the phenyl group. It is used in various applications, including as a fragrance ingredient and in the synthesis of other organic compounds. The compound's properties, such as its boiling point, solubility, and reactivity, are influenced by the presence of both the cyclohexyl and phenyl groups, making it a versatile building block in organic chemistry.

1152-58-5

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1152-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1152-58-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1152-58:
(6*1)+(5*1)+(4*5)+(3*2)+(2*5)+(1*8)=55
55 % 10 = 5
So 1152-58-5 is a valid CAS Registry Number.

1152-58-5Downstream Products

1152-58-5Relevant academic research and scientific papers

Visible light-induced transformation of aldehydes to esters, carboxylic anhydrides and amides

Gaspa, Silvia,Raposo, Inês,Pereira, Leonor,Mulas, Gabriele,Ricci, Pier Carlo,Porcheddu, Andrea,De Luca, Lidia

, p. 10711 - 10715 (2019)

A transition metal- and organophotocatalyst free synthesis of esters, carboxylic anhydrides and amides from aldehydes induced by visible-light has been reported. The proposed methodology can be carried out by the use of sunlight or artificial visible light as a blue LED source. The methodology has a very broad applicability and the desired products are obtained in very satisfactory yields.

Metal-Free Direct Oxidation of Aldehydes to Esters Using TCCA

Gaspa, Silvia,Porcheddu, Andrea,De Luca, Lidia

supporting information, p. 3666 - 3669 (2015/08/18)

Aromatic and aliphatic aldehydes are simply converted into esters by an efficient oxidative esterification carried out under mild conditions. The aldehydes are converted in situ into their corresponding acyl chlorides, which are then reacted with primary and secondary aliphatic, benzylic, allylic, and propargylic alcohols and phenols. A variety of esters are obtained in high yields.

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