55740-80-2

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
(S)-3-(isopropyl)pyridine is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its role in these applications is crucial for the development of new drugs and chemicals that can address various health and agricultural needs.
Used in the Food Industry:
In the food industry, (S)-3-(isopropyl)pyridine serves as a flavoring agent. Its unique properties contribute to enhancing the taste and aroma of various food products, making it a valuable component in the creation of flavors and fragrances.
Safety Precautions:
It is important to handle (S)-3-(isopropyl)pyridine with caution, as it may cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken to minimize any potential adverse effects during its use in different applications.

InChI:InChI=1/C8H11N/c1-7(2)8-4-3-5-9-6-8/h3-7H,1-2H3

Upstream product

• 97182-29-1 2-chloro-5-s-butylpyridine 
• 88488-68-0 2-s.butyl-5-nitropentanal diethylacetal 
• 69589-33-9 3-methyl-1-piperidino-1-pentene 
• 107-02-8 acrolein 
• 26871-37-4 (+)-(S)-2-s.butylsuccinaldehyde monodiethylacetal 
• 97182-28-0 (+)-(S)-5-sec-b utyl-2(1H)-pyridinone 
• 128776-22-7 3-sec-butyl-3,4-dihydro-2(1H)-pyridinone 
• 128776-14-7 (-)-(S)-3-sec-butyl-2(1H)-pyridinone 
• 5773-63-7 (+)-(S)-3-methylpentanenitrile 
• 128776-23-8 (+)-(S)-chloro-3-sec-butylpyridine 
• 88488-66-8 2-s.butyl-4-hydroxy-5-nitropentanal diethylacetal 
• 88488-67-9 2-s.butyl-5-nitro-4-pentenal diethylacetal 

Relevant academic research and scientific papers

Synthesis of (-)-(S)-3-sec-Butyl- and (+)-(S)-5-sec-Butyl-2(1H)-pyridinone.

Optically active (+)-(S)-5-sec-butyl- and (-)-(S)-3-sec-butyl-2(1H)-pyridinone are synthesized and the relationship between optical activity and minimum optical purity of the latter is determined.

OPTICALLY ACTIVE HETEROAROMATIC COMPOUNDS. IX. THE SYNTHESIS OF MONOALKYL-SUBSTITUTED OPTICALLY ACTIVE PYRIDINES

Optically active 2-, 3-, or 4-monoalkyl-substituted pyridines bearing the chirality centre at the alkyl group have been synthesized by several different synthetic procedures starting from easily available chiral synthons.Scopes and limitations of the synthetic methods as well as the relationships between the optical activity and the optical purity of the products are discussed.

Synthesis and Determination of Maximum Rotatory Power of (+)-(S)-5-s-Butyl-2(1H9-pyridinone

Optically active (S)-5-s-butyl-2(1H)-pyridinone (6) is obtained by reaction of 2-s-butylacrolein (1) and N-(carbamylmethyl)pyridinium chloride.The relationship between optical activity and minimum otical purity is determined.