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2-Pyridinamine,6-methyl-N-2-propenyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

222040-23-5

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222040-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 222040-23-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,0,4 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 222040-23:
(8*2)+(7*2)+(6*2)+(5*0)+(4*4)+(3*0)+(2*2)+(1*3)=65
65 % 10 = 5
So 222040-23-5 is a valid CAS Registry Number.

222040-23-5Downstream Products

222040-23-5Relevant academic research and scientific papers

Copper-catalyzed intramolecular dehydrogenative aminooxygenation: Direct access to formyl-substituted aromatic N-heterocycles

Wang, Honggen,Wang, Yong,Liang, Dongdong,Liu, Lanying,Zhang, Jiancun,Zhu, Qiang

supporting information; experimental part, p. 5678 - 5681 (2011/08/02)

A direct synthesis of carbaldehydes through intramolecular dehydrogenative aminooxygenation has been developed. The process uses a catalytic amount of copper(II) in DMF or DMA under oxygen and does not require additional oxidants (see scheme). Mechanistic studies suggest that the carbonyl oxygen atom of the aldehyde is derived from oxygen through a copper-mediated oxygen activation process via a peroxy-copper(III) intermediate. Copyright

Solid phase synthesis of aryl and heteroaryl amines using the Curtius rearrangement

Sunami, Satoshi,Sagara, Takeshi,Ohkubo, Mitsuru,Morishima, Hajime

, p. 1721 - 1724 (2007/10/03)

An efficient method for the solid phase synthesis of secondary aryl amines and heteroaryl amines was developed. The key step was the formation of aryl or heteroaryl carbamates using the Curtius rearrangement of aryl carboxylic acids with Wang resin as a trapping hydroxyl group. N-alkylation reactions of resin-bound carbamates under the Mitsunobu condition or using sodium hydride gave secondary aryl or heteroaryl amines in good yields. The developed method can be applied in the preparation of libraries containing aryl and heteroaryl amine structures as a pharmacophore.

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