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4-Ethyl-3-methyl-benzaldehyde is an organic compound with the chemical formula C11H12O. It is a derivative of benzaldehyde, featuring a benzene ring with an aldehyde group (-CHO) attached to the carbon atom at position 1. The molecule also has an ethyl group (-CH2CH3) at position 4 and a methyl group (-CH3) at position 3. This aromatic aldehyde is known for its strong, sweet, and floral odor, making it a valuable component in the fragrance industry. It is used in the production of perfumes, particularly in floral and fruity scents, as well as in the flavor industry to impart a characteristic aroma to food products. The compound can be synthesized through various chemical reactions, such as the Friedel-Crafts alkylation of tolualdehyde with ethyl halides. Due to its reactivity, 4-ethyl-3-methyl-benzaldehyde can also be used as a precursor in the synthesis of other organic compounds.

6521-18-2

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6521-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6521-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,2 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6521-18:
(6*6)+(5*5)+(4*2)+(3*1)+(2*1)+(1*8)=82
82 % 10 = 2
So 6521-18-2 is a valid CAS Registry Number.

6521-18-2Downstream Products

6521-18-2Relevant academic research and scientific papers

Direct transformation of simple enals to 3,4-disubstituted benzaldehydes under mild reaction conditions via an organocatalytic regio- and chemoselective dimerization cascade

Song, Xixi,Zhang, Xinshuai,Zhang, Shilei,Li, Hao,Wang, Wei

supporting information; experimental part, p. 9770 - 9774 (2012/08/28)

Straight to the point: An organocatalyzed, direct preparation of 3,4-disubstituted benzaldehydes from simple enals under mild conditions without the need for an additional oxidant has been developed. Notably, self-dimerization of an enal precursor and cro

Synthesis of aromatic aldehydes by organocatalytic [4+2] and [3+3] cycloaddition of α,β-unsaturated aldehydes

Hong, Bor-Cherng,Tseng, Hsing-Chang,Chen, Shang-Hung

, p. 2840 - 2850 (2007/10/03)

Organocatalytic inter- and intramolecular [4+2] and [3+3] cycloadditions of α,β-unsaturated aldehydes to give polysubstituted aromatic aldehydes are described. High periselectivity for the cycloadditions, with catalyst effects exerted by l-proline and pyrrolidine-HOAc, as well as cocatalyst, additive effects, has been observed.

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