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(1R,2S)-2-phenylcyclohex-3-enecarbaldehyde is a chiral organic compound with a molecular formula of C15H15O. It features a cyclohexene ring with a phenyl group attached to the 2nd carbon and a formyl group (aldehyde) at the 3rd carbon. The compound exhibits two chiral centers, which are the 1st and 2nd carbons, resulting in four possible stereoisomers. The specific configuration of (1R,2S)-2-phenylcyclohex-3-enecarbaldehyde is (1R,2S), indicating that the 1st carbon has an R configuration (hydrogen is on the right side when looking at the molecule) and the 2nd carbon has an S configuration (hydrogen is on the left side). (1R,2S)-2-phenylcyclohex-3-enecarbaldehyde is known for its unique aroma and is used in the synthesis of various fragrances and pharmaceuticals.

80825-32-7

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80825-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80825-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,2 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80825-32:
(7*8)+(6*0)+(5*8)+(4*2)+(3*5)+(2*3)+(1*2)=127
127 % 10 = 7
So 80825-32-7 is a valid CAS Registry Number.

80825-32-7Relevant academic research and scientific papers

Synthesis and anti-inflammatory activity of phenylbutenoid dimer analogs

Kim, Sung-Soo,Fang, Yuanying,Park, Haeil

supporting information, p. 1676 - 1680 (2015/07/15)

Several phenylbutenoid dimer (PBD) analogs were synthesized and evaluated for their inhibitory activities against nitric oxide (NO) production and TNF-α release. The PBD analogs were synthesized via Diels - Alder and subsequent Schlosser reactions as key steps. Among the tested compounds, two analogs (8c, 8f) exhibited much stronger inhibitory activity against LPS-stimulated NO production and TNF-α release in RAW 264.7 cells than that of wogonin.

CHEMISTRY OF ENOL ETHERS. LIII. PROTOTROPIC ISOMERIZATION IN THE SERIES OF CYCLIC 1-ALKOXY-1,4-DIENES

Makin, S. M.,Pomogaev, A. I.,Boiko, T. N.,Nikiforova, A. P.

, p. 2033 - 2036 (2007/10/02)

A series of diethyl acetals of 1-cyclohexene-3-carbaldehydes, the pyrolysis of which leads to the formation of cyclic 1-ethoxy-1,4-dienes, were obtained by the acetalization of 1-cyclohexene-3-carbaldehydes, which were obtained by the condensation of conjugated dienes with α,β-unsaturated aldehydes.The prototropic isomerization of the 1-ethoxy-1,4-dienes to corresponding 1-ethoxy-1,3-dienes under the influence of potassium tert-butoxide in dimethyl sulfoxide solution was investigated.

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