76006-14-9 Usage
General Description
3-Chloro-1H-pyrazolo[3,4-c]pyridine is a chemical compound with the molecular formula C7H4ClN3. It is a heterocyclic compound consisting of a pyrazole ring fused to a pyridine ring, with a chlorine atom attached to the third position of the pyrazole ring. 3-Chloro-1H-pyrazolo[3,4-c]pyridine is used in the synthesis of various pharmaceuticals and agricultural chemicals, as well as in organic chemistry research. It has the potential to exhibit diverse biological activities and is therefore of interest to researchers in the fields of medicinal chemistry and drug development. Additionally, its unique structure and properties make it a valuable building block for the construction of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 76006-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,0 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76006-14:
(7*7)+(6*6)+(5*0)+(4*0)+(3*6)+(2*1)+(1*4)=109
109 % 10 = 9
So 76006-14-9 is a valid CAS Registry Number.
76006-14-9Relevant articles and documents
Synthesis, reactivity and 13C-NMR of 1H-pyrazolo[3,4-c]pyridine derivatives
Milhavet, Jean-Claude,Gueiffier, Alain,Bernal, Lysiane,Teulade, Jean-Claude
, p. 1661 - 1667 (2007/10/03)
The synthesis of various 1H-pyrazolo [.-c.]pyridines was reported. 3- Cyano derivatives were obtained from the corresponding nitro compounds by Sandmeyer Reaction using Na3[Cu(CN)4] at pH 1. The 13C-NMR data of this series were also described.
Pyrazolopyridines. Part 5. Preparation and Reactions of Pyrazolopyridines
Chapman, David,Hurst, Jim
, p. 2398 - 2404 (2007/10/02)
A series of pyrazolopyridines has been prepared by nitrosation of 3-acetamido-4-methylpyridines and subsequent rearrangement and cyclisation of the N-acetyl-N-nitroso-compounds produced.The reactions of the pyrazolopyridines have been investigated. 1- and 2-Acetyl and 1- and 2-benzyl compounds were obtained and their structures elucidated spectroscopically.The ring system readily undergoes electrophilic substitution in the 3-position. 7-Chloropyrazolopyridine has been shown to be more susceptible to nucleophilic substitution than the isomeric 5-chloro-compound.
