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4-(1-ethyl-pentyl)-anisole, also known as 4-(1-ethylpentyl)phenyl methanol, is an organic compound with the chemical formula C14H22O. It is a colorless liquid with a mild, sweet, and floral odor. 4-(1-ethyl-pentyl)-anisole is primarily used as a fragrance ingredient in various consumer products, such as perfumes, cosmetics, and detergents. It is synthesized through the reaction of p-cresol with 1-ethyl-5-methylhexanal, and its molecular structure consists of a phenyl group attached to a methoxy group and a long alkyl chain. Due to its pleasant scent and stability, 4-(1-ethyl-pentyl)-anisole is a popular choice in the fragrance industry, although it is important to note that it should be used within safe concentration limits to avoid potential health risks.

7069-15-0

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7069-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7069-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7069-15:
(6*7)+(5*0)+(4*6)+(3*9)+(2*1)+(1*5)=100
100 % 10 = 0
So 7069-15-0 is a valid CAS Registry Number.

7069-15-0Relevant academic research and scientific papers

Iron-catalyzed alkylations of aromatic Grignard reagents

Cahiez, Gerard,Habiak, Vanessa,Duplais, Christophe,Moyeux, Alban

, p. 4364 - 4366 (2008/03/12)

(Chemical Equation Presented) Any old iron: Two efficient iron-catalyzed cross-coupling reactions between aryl Grignard reagents and alkyl bromides were developed that are suitable for large-scale applications. The first procedure uses iron acetylacetonate and involves a cooperative effect between the two ligands N,N,N′,N′-tetramethylethylenediamine (TMEDA) and hexamethylenetetraamine (HMTA), while the second procedure uses [(FeCl 3)2(tmeda)3] as catalyst. 2007 Wiley-VCH Verlag GmbH & Co. KGaA.

Reduction of Monobenzylic Alcohols with Sodium Borohydride/Trifluoroacetic Acid

Nutaitis, Charles F.,Bernardo, Joseph E.

, p. 487 - 493 (2007/10/02)

Sodium borohydride/trifluoroacetic acid readily effects the reduction of monobenzylic alcohols to afford the corresponding hydrocarbons in moderate to high yields.

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