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(R)-α-Phellandren-8-ol 3,5-dinitrobenzoate is a chiral compound derived from the monoterpene α-phellandrene, which is found in various essential oils, particularly in citrus fruits. The compound is characterized by the presence of a hydroxyl group at the 8th carbon position and a 3,5-dinitrobenzoate ester group attached to it. This esterification with 3,5-dinitrobenzoic acid enhances the compound's solubility in organic solvents and provides a chromophore, which can be useful for spectroscopic analysis. The (R)-enantiomer specifically refers to the configuration of the hydroxyl-bearing carbon, which is crucial for its biological activity and potential applications in the synthesis of pharmaceuticals and fragrances. (R)-α-phellandren-8-ol 3,5-dinitrobenzoate is of interest in the field of organic chemistry, particularly in the study of chiral molecules and their interactions.

2328-61-2

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2328-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2328-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,2 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2328-61:
(6*2)+(5*3)+(4*2)+(3*8)+(2*6)+(1*1)=72
72 % 10 = 2
So 2328-61-2 is a valid CAS Registry Number.

2328-61-2Downstream Products

2328-61-2Relevant academic research and scientific papers

Pheromone Synthesis, CIV.- Synthesis of the Enantiomers of α-Phellandren-8-ol (p-Mentha-1,5-dien-8-ol), a Monoterpene from Bark Beetles

Mori, Kenji,Igarashi, Yasuhiro

, p. 93 - 96 (2007/10/02)

Enantiomerically pure (R)-α-phellandren-8-ol (p-mentha-1,5-dien-8-ol, 1a) was synthesized from (R)-carvone (2).Similarly (S)-1a was synthesized from (S)-2.

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