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944-30-9

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944-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 944-30-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 944-30:
(5*9)+(4*4)+(3*4)+(2*3)+(1*0)=79
79 % 10 = 9
So 944-30-9 is a valid CAS Registry Number.

944-30-9Relevant articles and documents

Development of inhibitors of receptor protein tyrosine phosphatase β/ζ (PTPRZ1) as candidates for CNS disorders

Pastor, Miryam,Fernández-Calle, Rosalía,Di Geronimo, Bruno,Vicente-Rodríguez, Marta,Zapico, José María,Gramage, Esther,Coderch, Claire,Pérez-García, Carmen,Lasek, Amy W.,Puchades-Carrasco, Leonor,Pineda-Lucena, Antonio,de Pascual-Teresa, Beatriz,Herradón, Gonzalo,Ramos, Ana

, p. 318 - 329 (2018)

A new series of blood-brain barrier permeable molecules designed to mimic the activity of Pleiotrophin in the CNS has been designed and synthesized. These compounds exert their action by interacting with the intracellular domain PD1 of the Protein Tyrosin

Practical and efficient synthesis of aryl trifluoromethyl sulfones from arylsulfonyl chlorides with Umemoto's reagent II

Zhou, Xiaocong,Hu, Dufen,He, Xinyi,Li, Yuanqiang,Chu, Youqun,She, Yuanbin

supporting information, (2019/12/24)

A practical and efficient method for the synthesis of aryl trifluoromethyl sulfones has been developed by a tandem reaction of arylsulfonyl chlorides with Umemoto's reagent II. The advantageous features of this method are simple operation, mild reaction conditions, wide scope of substrates, high yield of products, and easy scalability.

Copper-catalyzed trifluoromethylation of arylsulfinate salts using an electrophilic trifluoromethylation reagent

Lin, Xiaoxi,Wang, Guimei,Li, Huaifeng,Huang, Yuanyuan,He, Weiming,Ye, Dandan,Huang, Kuo-Wei,Yuan, Yaofeng,Weng, Zhiqiang

, p. 2628 - 2632 (2013/03/29)

A copper-catalyzed method for the trifluoromethylation of arylsulfinates with Togni's reagent has been developed, affording aryltrifluoromethylsulfones in moderate to good yields. A wide range of functional groups in arylsulfinates are compatible with the

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