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N-hydroxy-2-(4-methoxyphenyl)-2-phenylacetimidoyl chloride is a complex organic chemical compound with the molecular formula C16H14ClNO3. It is a derivative of acetimidoyl chloride, featuring a hydroxyl group, a 4-methoxyphenyl group, and a phenyl group attached to the acetimidoyl moiety. N-hydroxy-2-(4-methoxyphenyl)-2-phenylacetimidoyl chloride is known for its reactivity and is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its ability to form amide bonds with other molecules. Its structure allows for the creation of new compounds with potential biological activity, making it a valuable building block in the field of organic synthesis.

4099-61-0

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4099-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4099-61-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4099-61:
(6*4)+(5*0)+(4*9)+(3*9)+(2*6)+(1*1)=100
100 % 10 = 0
So 4099-61-0 is a valid CAS Registry Number.

4099-61-0Relevant academic research and scientific papers

An efficient method for the synthesis of α-arylated nitroalkanes and α-arylated hydroximoyl chlorides mediated by AlCl3

Tu, Zhijay,Rama Raju,Liou, Tzuo-Rung,Kavala, Veerababurao,Kuo, Chun-Wei,Jang, Yaochung,Shih, Yu-Hsuan,Wang, Chun-Chao,Yao, Ching-Fa

experimental part, p. 2436 - 2442 (2009/07/25)

Friedel-Crafts alkylation of various arenes/heteroarenes to β-nitrostyrenes mediated by aluminum chloride is described. The interesting feature of this methodology pertain the formation of different products by tuning the reaction temperature. α-Arylated

Intermolecular Diastereoselective Nitrile Oxide Addition With Propargylic Ethers

Baskaran, Subramanian,Baskaran, Chitra,Trivedi, Girish K.

, p. 2459 - 2471 (2007/10/03)

With simple and stereogenic propargylic ethers 3,4,5,7 and 11, cycloaddition reactions of the nitrile oxide 2 are performed in moderately high yield and with considerable regioselectivity.

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