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3,4-Dimethoxy-benzoesaeure-p-toluidid, also known as 3,4-dimethoxybenzoic acid p-toluidide, is a chemical compound with the molecular formula C15H17NO4. It is a derivative of benzoic acid, featuring two methoxy groups at the 3rd and 4th carbon positions and a p-toluidide group attached to the carboxyl group. This organic compound is characterized by its aromatic structure and is used in various chemical reactions and synthesis processes. It is an important intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique functional groups and reactivity.

1522-72-1

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1522-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1522-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1522-72:
(6*1)+(5*5)+(4*2)+(3*2)+(2*7)+(1*2)=61
61 % 10 = 1
So 1522-72-1 is a valid CAS Registry Number.

1522-72-1Downstream Products

1522-72-1Relevant academic research and scientific papers

Nickel-Catalyzed Denitrogenative Cross-Coupling Reaction of 1,2,3-Benzotriazin-4(3 H)-ones with Organoboronic Acids: An Easy Access to Ortho-Arylated and Alkenylated Benzamides

Hari Balakrishnan, Madasamy,Sathriyan, Kotturaja,Mannathan, Subramaniyan

, p. 3815 - 3818 (2018)

A novel nickel-catalyzed approach to synthesize ortho-arylated and alkenylated benzamides in good to high yields via a denitrogenative cross-coupling reaction of 1,2,3-benzotriazin-4(3H)-ones with organoboronic acids is described. The reaction proceeds th

Imidazolium-supported benzotriazole: an efficient and recoverable activating reagent for amide, ester and thioester bond formation in water

Shakoor, S.M. Abdul,Choudhary, Sunita,Bajaj, Kiran,Muthyala, Manoj Kumar,Kumar, Anil,Sakhuja, Rajeev

, p. 82199 - 82207 (2015/10/12)

An efficient and recyclable imidazolium-supported benzotriazole reagent (Im-CH2-BtH) as a novel synthetic auxiliary has been synthesized and its utility as a carboxyl group activating reagent via the formation of stable imidazolium-supported acyl benzotriazoles was explored for the synthesis of amides, esters and thioesters in water under microwave conditions. The reagent was reused five times without any noticeable loss in activity. It is moisture insensitive and highly stable under thermal and aerobic conditions. The application of imidazolium-supported N-acetyl benzotriazole leads to synthesis of paracetamol on the gram scale under greener conditions in 93% yield.

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