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(+/-)-6-Hydroxy-6-phenyl-hexansaeure-aethylester, also known as (±)-ethyl 6-hydroxy-6-phenylhexanoate, is a chiral organic compound with the molecular formula C14H18O3. It is a colorless liquid with a fruity, floral odor and is commonly used as a fragrance ingredient in various cosmetic and personal care products. (+/-)-6-Hydroxy-6-phenyl-hexansaeure-aethylester is characterized by its hydroxyl group, phenyl ring, and hexanoate chain, which contribute to its unique chemical properties and applications. It is synthesized through various chemical reactions, such as the condensation of phenylacetaldehyde with ethyl acetoacetate, followed by hydrolysis and esterification. Due to its chiral nature, it exists as a mixture of two enantiomers, which can have different biological activities and sensory properties.

4066-98-2

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4066-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4066-98-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4066-98:
(6*4)+(5*0)+(4*6)+(3*6)+(2*9)+(1*8)=92
92 % 10 = 2
So 4066-98-2 is a valid CAS Registry Number.

4066-98-2Relevant academic research and scientific papers

Remote Reformatsky Reaction: Reaction of β-, γ-, and δ-Zinc Esters with Aldehydes

Tamaru, Y.,Nakamura, T.,Sakaguchi, M.,Ochiai, H.,Yoshida, Z.

, p. 610 - 611 (1988)

Ethyl β-, γ-, and δ-zinc esters react with aldehydes to provide ethyl γ-, δ-, and ε-hydroxy esters.

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