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α,α-Dimethyl-1-cyclohexene-1-acetic acid is a synthetic organic compound with the chemical formula C10H16O2. It is a derivative of cyclohexane, featuring a cyclohexene ring with a methyl group at each of the alpha positions (adjacent to the double bond) and an acetic acid group attached to the carbon atom of the double bond. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can be used as an intermediate in the production of compounds with biological activity, such as certain types of insecticides and pharmaceuticals. The compound's properties, such as its lipophilicity and ability to form stable derivatives, make it a valuable building block in organic synthesis.

16642-55-0

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16642-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16642-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,4 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16642-55:
(7*1)+(6*6)+(5*6)+(4*4)+(3*2)+(2*5)+(1*5)=110
110 % 10 = 0
So 16642-55-0 is a valid CAS Registry Number.

16642-55-0Relevant academic research and scientific papers

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

-

, (2015/02/02)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

SYNTHETIS OF CYCLIC AND ACYCLIC β,γ-UNSATURATED CARBOXYLIC ACIDS VIA AN E1-TYPE IONIZATION/ELIMINATION OF β-LACTONES

Black, T. Howard,Eisenbeis, Shane A.,McDermott, Todd S.,Maluleka, Stephen L.

, p. 2307 - 2316 (2007/10/02)

Cyclic and acyclic ketones were converted in three steps into 3-alkenoic acids, bearing a variety of substituents in the α-position.The sequence, involving ionization/elimination of a β-lactone, affords high yields of pure products uncontaminated with conjugated isomers.Support for an E1-type mechanism is also provided.

A NOVEL SYNTHESIS OF MONO- AND DISUBSTITUTED (1-CYCLOALKENYL) ACETIC ACID DERIVATIVES VIA IONIZATION/ELIMINATION OF β-LACTONES

Black, T. Howard,Eisenbeis, Shane

, p. 2243 - 2248 (2007/10/02)

Spiro β-lactones undergo an ionization/elimination reaction to afford cycloalkenyl acetic acid derivatives in high yield and isomeric purity.

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