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N-[(3-methylphenyl)(phenyl)methyl]acetamide is a chemical compound with the molecular formula C17H17NO. It is a derivative of acetamide, featuring a 3-methylphenyl group and a phenyl group attached to the nitrogen atom. N-[(3-methylphenyl)(phenyl)methyl]acetamide is an aromatic amide, characterized by the presence of an amide functional group (-CONH-) and two aromatic rings. It is a white crystalline solid and is used in various applications, including pharmaceuticals and chemical research. The compound's structure provides it with unique properties, such as its ability to form hydrogen bonds and its potential for use in the synthesis of other organic compounds.

5580-52-9

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5580-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5580-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5580-52:
(6*5)+(5*5)+(4*8)+(3*0)+(2*5)+(1*2)=99
99 % 10 = 9
So 5580-52-9 is a valid CAS Registry Number.

5580-52-9Downstream Products

5580-52-9Relevant academic research and scientific papers

Bis-sulfamyl imines: Potent substrates for asymmetric additions of arylboroxines under rhodium catalysis

Crampton, Rosemary,Woodward, Simon,Fox, Martin

supporting information; experimental part, p. 903 - 906 (2011/06/19)

Bis-sulfamyl imines are shown to be potentially ideal substrates for rhodium-catalysed asymmetric additions of arylboron nucleophiles as they show: (i) near perfect enantioselectivities (11 examples, 98-99+% ee), (ii) good to excellent diastereoselectivities (10-32:1 rac:meso), and (iii) high functional group tolerance in removal of the low molecular weight protecting group via mild heating in aqueous pyridine.

α-Amidobenzylation of aryl and alkenyl halides via palladium-catalyzed Suzuki-Miyaura coupling with α-(acylamino) benzylboronic esters

Ohmura, Toshimichi,Awano, Tomotsugu,Suginome, Michinori

supporting information; experimental part, p. 664 - 665 (2011/04/22)

The Suzuki-Miyaura coupling of α-(acetylamino)benzylboronic esters with aryl and alkenyl halides has been achieved using a Pd/P(t-Bu)3 catalyst with KF and H2O in 1,4-dioxane, giving α-substituted benzylamines in high yields. Copyright

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