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4-(3,5-dimethylphenyl)butan-2-ol, also known as 4-(3,5-dimethylphenyl)-2-butanol, is an organic compound with the molecular formula C12H18O. It is a colorless liquid with a molecular weight of 178.27 g/mol. 4-(3,5-dimethylphenyl)butan-2-ol is characterized by a butanol backbone, with a 3,5-dimethylphenyl group attached at the 4-position. The 3,5-dimethylphenyl group consists of a benzene ring with two methyl groups attached at the 3rd and 5th carbon atoms. 4-(3,5-dimethylphenyl)butan-2-ol is used as a fragrance ingredient and can be found in various consumer products such as perfumes, cosmetics, and personal care items. It is synthesized through chemical reactions and is known for its pleasant, floral scent.

1250606-63-3

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1250606-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1250606-63-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,0,6,0 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1250606-63:
(9*1)+(8*2)+(7*5)+(6*0)+(5*6)+(4*0)+(3*6)+(2*6)+(1*3)=123
123 % 10 = 3
So 1250606-63-3 is a valid CAS Registry Number.

1250606-63-3Downstream Products

1250606-63-3Relevant academic research and scientific papers

"One-pot" tandem C - H borylation/1,4-conjugate addition/reduction sequence

Tajuddin, Hazmi,Shukla, Lena,Maxwell, Aoife C.,Marder, Todd B.,Steel, Patrick G.

, p. 5700 - 5703 (2011/03/19)

A microwave-assisted, one-pot, iridium-catalyzed aromatic C - H borylation/rhodium-catalyzed 1,4-conjugate addition sequence provides a highly robust protocol suitable for high-throughput array synthesis. Selective formation of either β-aryl-substituted ketones or the corresponding alcohols can be achieved in good overall yields by simple variation of the reaction conditions.

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