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Benzyl-heptyl-malonic acid is a complex organic compound with the molecular formula C17H24O4. It is a derivative of malonic acid, featuring a benzyl group (C6H5-CH2-) and a heptyl chain (C7H15-) attached to the malonic acid backbone. benzyl-heptyl-malonic acid is characterized by its ester-like structure, which consists of a carbonyl group (C=O) bonded to two alkyl or aryl groups. Benzyl-heptyl-malonic acid is synthesized through a series of chemical reactions, often involving the condensation of malonic acid with benzyl and heptyl halides or alcohols. It has potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs, fragrances, and other specialty chemicals. Due to its unique structure, it may exhibit specific properties, such as solubility in organic solvents and reactivity with nucleophiles, which can be exploited in various chemical transformations.

4379-26-4

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4379-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4379-26-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4379-26:
(6*4)+(5*3)+(4*7)+(3*9)+(2*2)+(1*6)=104
104 % 10 = 4
So 4379-26-4 is a valid CAS Registry Number.

4379-26-4Relevant academic research and scientific papers

Synthesis and olfactory evaluation of optically active β-alkyl substituted γ-lactones and whiskey lactone analogues

Kato, Daiki,Kawasaki, Masashi,Morita, Yuko,Okada, Takuya,Tanaka, Yasuo,Toyooka, Naoki

, (2020/02/22)

Optically active β-alkyl substituted γ-lactones and whiskey lactone analogues were synthesized, and the odor properties were evaluated. During the preparation of the chiral intermediates, we found good reaction conditions for the highly enantioselective esterification of 3-arylmethyl-2-methyl-1-propanols to kinetically resolve them. The results of the olfactory evaluations of the synthesized lactones revealed that the alkyl groups on the γ-lactone rings played an important role for the odor profiles.

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