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Cyclohexanecarboxaldehyde, 4-methyl-cis, is an organic compound with the chemical formula C8H14O. It is a cyclic aldehyde with a methyl group attached to the fourth carbon atom in the cyclohexane ring. Cyclohexanecarboxaldehyde, 4-methyl-, cis- is characterized by its cis-configuration, meaning that the double bond between the carbonyl group and the cyclohexane ring is in the same plane, resulting in a specific geometric arrangement of the molecule. It is an important intermediate in the synthesis of various pharmaceuticals, fragrances, and agrochemicals due to its unique structure and reactivity. Cyclohexanecarboxaldehyde, 4-methyl-cis, is typically synthesized through various chemical reactions, such as the hydroformylation of 4-methylcyclohexene, and is known for its distinct chemical properties and potential applications in the chemical industry.

7133-04-2

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7133-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7133-04-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7133-04:
(6*7)+(5*1)+(4*3)+(3*3)+(2*0)+(1*4)=72
72 % 10 = 2
So 7133-04-2 is a valid CAS Registry Number.

7133-04-2Downstream Products

7133-04-2Relevant academic research and scientific papers

IL-17 Ligands And Uses Thereof

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Paragraph 1003-1004, (2020/08/20)

Provided herein are novel ligands and pharmaceutical compositions thereof which modulate IL-17A. Also provided are methods for preparing the IL-17A modulators. Such compounds may be useful in the treatment and/or prevention of, for example, inflammation, cancer or autoimmune disease.

Axial and equatorial cyclohexylacyl and tetrahydropyranyl-2-acyl radicals. An experimental and theoretical study

DiLabio, Gino A.,Ingold, Keith U.,Roydhouse, Mark D.,Walton, John C.

, p. 4319 - 4322 (2007/10/03)

(Chemical Equation Presented) Axial and equatorial cyclohexylacyl and tetrahydropyranyl-2-acyl radicals gave distinct EPR spectra thanks to surprisingly large β-hydrogen atom hyperfine splittings that enabled them to be characterized and monitored. DFT computations indicated that the axial species (X = CH2) had a higher barrier to rotation about the (O)Cα-Cα bond. The computed difference ΔH° for the axial and equatorial radicals (R = H, X = CH2) was 0.8 kcal mol -1.

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