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C2H4O2*C12H6F5N3O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1280708-38-4

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1280708-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1280708-38-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,0,7,0 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1280708-38:
(9*1)+(8*2)+(7*8)+(6*0)+(5*7)+(4*0)+(3*8)+(2*3)+(1*8)=154
154 % 10 = 4
So 1280708-38-4 is a valid CAS Registry Number.

1280708-38-4Downstream Products

1280708-38-4Relevant articles and documents

Binding of polyatomic anions with protonated ureido-pyridyl ligands

Marivel,Arunachalam,Ghosh, Pradyut

, p. 1642 - 1650 (2011)

Two ureido-pyridyl ligands, 1-(4-nitro-phenyl)-3-pyridine-3-ylmethyl-urea (L1) and 1-pentafluorophenyl-3-pyridine-4-yl-urea (L2) were synthesized in good yields, and solid-state anion binding studies of (HL1)+ and (HL2)+ with polyatomic anions such as NO3-, AcO-, ClO4 -, SO42-, and SiF62- were carried out in detail. Protonation of the pyridyl nitrogen center of L 1 with HNO3, HClO4, and HF in different solvent media yielded crystals of complexes 1 (HL1 · NO3), 2 (HL1 · ClO4), and 3 (HL1 · 0.5SiF6) suitable for single crystal X-ray diffraction studies, respectively. Similarly, protonation of L2 with HNO3, CH3COOH, and H2SO4 yielded single crystals of complexes 4 [2(HL2 · NO3) ·DMF], 5 (HL 2 · AcO), and 6 [(HL2)2 · SO 4], respectively. X-ray crystallographic analysis of all these six complexes has been carried out and the details of anion binding with the urea functionality of ureido-pyridyl ligands were investigated. In all the complexes, the pyridyl moiety of the ligands is found to be protonated and the binding of anions are observed at the urea functionality of the ligands through the R 22(8) hydrogen bonding motif irrespective of sizes and shapes of anions or the electron withdrawing ability of aryl substitutions (p-nitro phenyl vs pentafluoro phenyl) or the position of the pyridyl nitrogen center (protonation site) of the designed ligands.

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