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1623809-04-0

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1623809-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1623809-04-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,3,8,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1623809-04:
(9*1)+(8*6)+(7*2)+(6*3)+(5*8)+(4*0)+(3*9)+(2*0)+(1*4)=160
160 % 10 = 0
So 1623809-04-0 is a valid CAS Registry Number.

1623809-04-0Relevant articles and documents

Palladium-Catalyzed Ring-Forming Alkene Aminoaroylation of Unsaturated Hydrazones and Sulfonamides

Chen, Jun,Yang, Meng-Nan,Chen, Jia-Rong,Xiao, Wen-Jing

supporting information, p. 3314 - 3318 (2018/06/11)

The first example of a Pd(OAc)2-catalyzed ring-forming alkene aminoaroylation of unsaturated hydrazones and sulfonamides is described. This protocol features the use of diaryliodonium salts as both oxidants and aryl sources, thus enabling mild

PhI(OAc)2-mediated functionalisation of unactivated alkenes for the synthesis of pyrazoline and isoxazoline derivatives

Hu, Xiao-Qiang,Feng, Guoqiang,Chen, Jia-Rong,Yan, Dong-Mei,Zhao, Quan-Qing,Wei, Qiang,Xiao, Wen-Jing

supporting information, p. 3457 - 3461 (2015/03/18)

A PhI(OAc)2-promoted radical cyclization of β,γ-unsaturated hydrazones and oximes has been developed for an efficient synthesis of various valuable pyrazoline and isoxazoline derivatives with satisfactory yields (up to 96%) under mild condition

Photocatalytic Generation of N-Centered Hydrazonyl Radicals: A Strategy for Hydroamination of β,γ-Unsaturated Hydrazones

Hu, Xiao-Qiang,Chen, Jia-Rong,Wei, Qiang,Liu, Feng-Lei,Deng, Qiao-Hui,Beauchemin, André M.,Xiao, Wen-Jing

supporting information, p. 12163 - 12167 (2016/02/23)

A visible-light photocatalytic generation of N-centered hydrazonyl radicals has been accomplished for the first time. This approach allows efficient intramolecular addition of hydrazonyl radical to terminal alkenes, thus providing hydroamination and oxyamination products in good yields. Importantly, the protocol involves deprotonation of an N-H bond and photocatalytic oxidation to an N-centered radical, thus obviating the need to prepare photolabile amine precursors or the stoichiometric use of oxidizing reagents.

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