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1-(4-methoxy-3-methylphenyl)-2-phenylbutan-1-one is a complex organic compound with the molecular formula C18H20O2. It features a butanone functional group, which is a four-carbon ketone, with a phenyl group attached to the second carbon. One of the phenyl rings has a 4-methoxy substituent, which is a methoxy group (-OCH3) attached to the fourth carbon, and a 3-methyl substituent, which is a methyl group (-CH3) attached to the third carbon. The other phenyl ring is unsubstituted. 1-(4-methoxy-3-methylphenyl)-2-phenylbutan-1-one is known for its potential applications in the synthesis of various pharmaceuticals and fragrances due to its unique structure and properties.

1979-67-5

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1979-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1979-67-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1979-67:
(6*1)+(5*9)+(4*7)+(3*9)+(2*6)+(1*7)=125
125 % 10 = 5
So 1979-67-5 is a valid CAS Registry Number.

1979-67-5Downstream Products

1979-67-5Relevant academic research and scientific papers

In(III)-mediated chemoselective dehydrogenative interaction of ClMe 2SiH with carboxylic acids: Direct chemo- And regioselective friedel-crafts acylation of aromatic ethers

Babu, Srinivasarao Arulananda,Yasuda, Makoto,Baba, Akio

, p. 405 - 408 (2007)

Chemoselective dehydrogenative interaction of ClMe2SiH with a carboxylic acid group in the presence of InX3 is reported. 13C NMR investigation revealed the formation of PhCOOSi(Cl)Me 2as the major transient intermediate. Chemo- and regioselective Friedel-Crafts acylation of aromatic ethers directly from carboxylic acids was established.

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