4072-13-3 Usage
Description
(2-methoxy-5-methylphenyl)(phenyl)methanone is a chemical compound characterized by a benzene ring with a methoxy group and a methyl group substitution. It features a ketone functional group attached to the benzene ring, which contributes to its unique structure and reactivity.
Uses
Used in Pharmaceutical Industry:
(2-methoxy-5-methylphenyl)(phenyl)methanone is used as an intermediate or building block in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (2-methoxy-5-methylphenyl)(phenyl)methanone serves as a key intermediate in the production of agrochemicals. Its properties allow for the creation of effective compounds used in agriculture.
Used in Dye Industry:
(2-methoxy-5-methylphenyl)(phenyl)methanone is utilized as a precursor in the synthesis of dyes. Its molecular structure contributes to the color and properties of the resulting dyes, making it an important component in this industry.
Used in Research and Industrial Processes:
Due to its unique structure and reactivity, (2-methoxy-5-methylphenyl)(phenyl)methanone has potential applications in various research and industrial processes. It can be employed in the development of new materials and chemical reactions.
It is important to follow proper safety protocols when handling and using (2-methoxy-5-methylphenyl)(phenyl)methanone to prevent any potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 4072-13-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4072-13:
(6*4)+(5*0)+(4*7)+(3*2)+(2*1)+(1*3)=63
63 % 10 = 3
So 4072-13-3 is a valid CAS Registry Number.
4072-13-3Relevant articles and documents
NOVEL PROCESS FOR THE PREPARATION OF TOLTERODINE
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Page/Page column 13-14, (2010/11/26)
The present invention relates to a novel and improved process for the preparation of tolterodine of formula I. Key steps involved in the process are a vinyl Grignard reaction on a benzophenone derivative of formula XXI to get the vinyl carbinol derivative
METHOD OF OBTAINING TOLTERODINE
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Page/Page column 8, (2008/06/13)
The process comprises reacting a compound of formula (II), where R is a hydroxyl protecting group, and the asterisk indicates an asymmetric carbon atom, with diisopropylamine in the presence of a reducing agent; optionally converting the resulting intermediate into a salt and, if so desired, isolating it; removing the hydroxyl protecting group; and if so desired, separating the desired (R) or (S) enantiomer, or the mixture of enantiomers and/or converting the obtained compound into a pharmaceutically acceptable salt thereof. Tolterodine is a muscarinic receptor antagonist useful in treating urinary incontinence and other symptoms of urinary bladder hyperactivity.
Aluminum dodecatungstophosphate (AlPW12O40) as a non-hygroscopic Lewis acid catalyst for the efficient Friedel-Crafts acylation of aromatic compounds under solvent-less conditions
Firouzabadi, Habib,Iranpoor, Nasser,Nowrouzi, Farhad
, p. 10843 - 10850 (2007/10/03)
Stable and non-hygroscopic aluminum dodecatungstophosphate (AlPW 12O40), which is prepared easily from cheap and commercially available compounds was found to be an effective catalyst for Friedel-Crafts acylation reactions using carboxylic acids, acetic anhydride and benzoyl chloride in the absence of solvent under mild reaction conditions.
