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Benzene, 2-hexyl-1,4-dimethyl-, also known as 1,4-dimethyl-2-hexylbenzene, is an organic compound with the chemical formula C14H22. It is a derivative of benzene, featuring a benzene ring with two methyl groups attached at the 1st and 4th carbon atoms, and a hexyl chain (six-carbon alkyl group) attached at the 2nd carbon atom. Benzene, 2-hexyl-1,4-dimethyl- is a colorless liquid with a mild aromatic odor and is used as a solvent, fragrance component, and intermediate in the synthesis of various chemicals. It is insoluble in water but soluble in organic solvents, and its physical properties include a boiling point of approximately 260°C and a density of around 0.85 g/cm3. Due to its potential health and environmental risks, handling and disposal of this chemical should be done with proper safety measures and in accordance with local regulations.

3042-53-3

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3042-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3042-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,4 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3042-53:
(6*3)+(5*0)+(4*4)+(3*2)+(2*5)+(1*3)=53
53 % 10 = 3
So 3042-53-3 is a valid CAS Registry Number.

3042-53-3Downstream Products

3042-53-3Relevant academic research and scientific papers

Novel acidic ionic liquids catalytic systems for friedel-crafts alkylation of aromatic compounds with alkenes

Qiao, Kun,Yokoyama, Chiaki

, p. 472 - 473 (2007/10/03)

Novel acidic ionic liquids catalytic systems are developed for the Friedel-Crafts alkylation of aromatic compounds with alkenes.

Integrated chemical process: One-pot aromatization of cyclic enones by the double elimination methodology

Orita, Akihiro,Yaruva, Jayamma,Otera, Junzo

, p. 2267 - 2270 (2007/10/03)

A variety of aromatic hydrocarbons bearing multiple alkyl substituents are accessible with perfect regiocontrol in a one-pot reaction starting from cyclo-hexenones and their aromatic analogues [Eq. (1)]. The present methodology can be further extended to the synthesis of polycyclic aromatic hydrocarbons. The drawbacks encountered in the Friedel-Crafts reaction are resolved since the reaction proceeds under basic conditions.

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