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2-((S)-1-Hydroxy-ethyl)-pentanoic acid ethyl ester, also known as ethyl (S)-2-hydroxyethylpentanoate, is an organic compound with the molecular formula C9H18O3. It is a chiral ester derived from pentanoic acid, featuring a hydroxyethyl group attached to the second carbon of the pentanoic acid chain. 2-((S)-1-Hydroxy-ethyl)-pentanoic acid ethyl ester is characterized by its asymmetric carbon center, which gives rise to two enantiomers, with the (S)-configuration being the specific form mentioned. It is used in the synthesis of various pharmaceuticals and chemical compounds due to its unique structural properties. The ester group in 2-((S)-1-Hydroxy-ethyl)-pentanoic acid ethyl ester allows for potential hydrolysis reactions, making it a versatile building block in organic chemistry.

39788-63-1

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39788-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39788-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,8 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39788-63:
(7*3)+(6*9)+(5*7)+(4*8)+(3*8)+(2*6)+(1*3)=181
181 % 10 = 1
So 39788-63-1 is a valid CAS Registry Number.

39788-63-1Downstream Products

39788-63-1Relevant academic research and scientific papers

Chemo-enzymatic alkylation of active methylene compounds

Fuganti,Pedrocchi-Fantoni,Servi

, p. 4195 - 4198 (2007/10/02)

Active methylene compounds undergo chemical condensation in water with aldehydes derived from yeast oxidation of the corresponding alcohols. Unsaturated compounds so obtained are then further reduced by yeast.

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