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(S)-4-isopropyl-2-(pyrazin-2-yl)-4,5-dihydrooxazole is a heterocyclic chemical compound with the molecular formula C12H16N4O. It features both a pyrazine and an oxazole ring, and an isopropyl group attached to the second carbon. As a dihydrooxazole, it has a double bond between the fourth and fifth carbon atoms in the oxazole ring. This organic molecule may hold potential applications in pharmaceutical and medicinal chemistry due to its unique structure and possible biological activity.

2757082-79-2

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2757082-79-2 Usage

Uses

Used in Pharmaceutical Industry:
(S)-4-isopropyl-2-(pyrazin-2-yl)-4,5-dihydrooxazole is used as a potential pharmaceutical compound for its heterocyclic nature and possible biological activity. Its unique structure may allow it to interact with various biological targets, making it a candidate for the development of new drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-4-isopropyl-2-(pyrazin-2-yl)-4,5-dihydrooxazole is used as a building block or a scaffold for designing new molecules with therapeutic potential. Its heterocyclic structure can be further modified or functionalized to enhance its biological activity and target specific receptors or enzymes in the body.

Check Digit Verification of cas no

The CAS Registry Mumber 2757082-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,7,5,7,0,8 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2757082-79:
(9*2)+(8*7)+(7*5)+(6*7)+(5*0)+(4*8)+(3*2)+(2*7)+(1*9)=212
212 % 10 = 2
So 2757082-79-2 is a valid CAS Registry Number.

2757082-79-2Downstream Products

2757082-79-2Relevant academic research and scientific papers

Efficacious and rapid metal- and solvent-free synthesis of enantiopure oxazolines

Hassani, Rym,Requet, Alexandre,Marque, Sylvain,Gaucher, Anne,Prim, Damien,Kacem, Yakdhane,Hassine, Bchir Ben

, p. 1275 - 1279 (2014)

A rapid and efficient synthesis of oxazolines was performed starting from various nitriles using microwave irradiation combined to metal- and solvent-free conditions to afford high to quantitative yields of the targeted heterocycles.

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