120234-29-9 Usage
General Description
(2-Chloro-pyridin-3-yl)-diMethyl-aMine is a chemical compound with the molecular formula C7H9ClN2. It is a derivative of pyridine and contains a chloro and dimethylamine group on the 3-position of the pyridine ring. (2-Chloro-pyridin-3-yl)-diMethyl-aMine is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active compounds. It is also used as an intermediate in the production of agrochemicals and pharmaceuticals. The compound is a clear, colorless liquid at room temperature and should be handled with care due to its toxic and potentially hazardous nature.
Check Digit Verification of cas no
The CAS Registry Mumber 120234-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,3 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120234-29:
(8*1)+(7*2)+(6*0)+(5*2)+(4*3)+(3*4)+(2*2)+(1*9)=69
69 % 10 = 9
So 120234-29-9 is a valid CAS Registry Number.
120234-29-9Relevant articles and documents
[FeFe]-Hydrogenase Mimic Employing κ2-C,N-Pyridine Bridgehead Catalyzes Proton Reduction at Mild Overpotential
Schippers, Esther C. F.,Nurttila, Sandra S.,Oudsen, Jean-Pierre H.,Tromp, Moniek,Dzik, Wojciech I.,van der Vlugt, Jarl Ivar,Reek, Joost N. H.
, p. 2510 - 2517 (2019)
Two novel κ2-C,N-pyridine bridged [FeFe]-H2ase mimics (1 and 2) have been prepared and are shown to function as efficient molecular catalysts for electrocatalytic proton reduction. The elemental and structural composition of the complexes are confirmed by NMR and IR spectroscopy, high-resolution mass spectrometry and single-crystal X-ray diffraction. Electrochemical investigations reveal that the complexes reduce protons at their first reduction potential, resulting in the lowest overpotential (120 mV) ever reported for [FeFe]-H2ase mimics in proton reduction catalysis when mild acid (phenol) is used as proton source.
