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"Acetat v. 2-Methyl-3-<4-isopropyl-phenyl>-propen-(1)-ol-(1)" is a complex chemical compound with the molecular formula C16H22O2. It is an ester derivative of 2-methyl-3-(4-isopropylphenyl)propen-1-ol, which is a type of alcohol. Acetat v. 2-Methyl-3-<4-isopropyl-phenyl>-propen-(1)-ol-(1) is characterized by its unique structure, featuring a 2-methyl-3-phenylpropen-1-ol core with an isopropyl group attached to the phenyl ring. The acetate group is esterified to the hydroxyl group of the alcohol, enhancing its reactivity and solubility properties. This chemical is often used in the synthesis of various pharmaceuticals and fragrances due to its distinctive chemical properties and potential applications in the creation of new compounds with specific therapeutic or sensory effects.

6839-77-6

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6839-77-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6839-77-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6839-77:
(6*6)+(5*8)+(4*3)+(3*9)+(2*7)+(1*7)=136
136 % 10 = 6
So 6839-77-6 is a valid CAS Registry Number.

6839-77-6Downstream Products

6839-77-6Relevant academic research and scientific papers

An efficient TiCl4-catalysed method for the synthesis of para-substituted aromatic aldehydes

Zhou, Chenfeng,Su, Weike

, p. 555 - 557 (2015/11/27)

An efficient and highly selective synthesis of para-substituted aromatic aldehydes has been achieved by TiCl4-catalysed Friedel-Crafts alkylation of monosubstituted benzenes with methacrolein diacetyl acetal.

Precursor compounds

-

, (2008/06/13)

The compounds of the formula I are precursors for organoleptic and antimicrobial compounds. The latter are generated in the presence of skin bacteria, enzymes or acidic or alkaline conditions. One precursor molecule can provide one or more different compounds.

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