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(4-cyclopentylbutyl)benzene is an organic compound with the molecular formula C17H24. It is a derivative of benzene, featuring a cyclopentylbutyl group attached to the benzene ring. (4-cyclopentylbutyl)benzene is characterized by its unique structure, which combines the aromatic nature of benzene with the aliphatic chain of cyclopentylbutyl. It is a colorless liquid with a distinct aromatic odor and is insoluble in water but soluble in organic solvents. (4-cyclopentylbutyl)benzene has potential applications in the synthesis of various chemical compounds and pharmaceuticals, as well as in the fragrance industry due to its pleasant scent.

5716-74-5

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5716-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5716-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5716-74:
(6*5)+(5*7)+(4*1)+(3*6)+(2*7)+(1*4)=105
105 % 10 = 5
So 5716-74-5 is a valid CAS Registry Number.

5716-74-5Relevant academic research and scientific papers

PHOTOCATALYST SYSTEM AND USE THEREOF IN A PHOTOCATALYTIC PROCESS

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Page/Page column 33; 38-40, (2019/06/13)

Photocatalyst system and use thereof in a photochemical process The invention relates to a photocatalyst system comprising, in the absence of a further photosensitizer other than the compound of formula (III) or a mixture thereof: (i) a nickel(II) salt, (

Formation of C(sp3)–C(sp3) Bonds through Nickel-Catalyzed Decarboxylative Olefin Hydroalkylation Reactions

Lu, Xi,Xiao, Bin,Liu, Lei,Fu, Yao

supporting information, p. 11161 - 11164 (2016/08/03)

Olefins and carboxylic acids are among the most important feedstock compounds. They are commonly found in natural products and drug molecules. We report a new reaction of nickel-catalyzed decarboxylative olefin hydroalkylation, which provides a novel practical strategy for the construction of C(sp3)?C(sp3) bonds. This reaction can tolerate a variety of synthetically relevant functional groups and shows good chemo- and regioselectivity. It enables cross-coupling of complex organic molecules containing olefin groups and carboxylic acid groups in a convergent fashion.

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