29620-66-4 Usage
General Description
2-Methyl-quinoline-4-carboxylic acid hydrazide is a chemical compound with potential applications in pharmaceuticals and organic synthesis. It is a hydrazide derivative of 2-methyl-quinoline-4-carboxylic acid, containing a hydrazine functional group. 2-METHYL-QUINOLINE-4-CARBOXYLIC ACID HYDRAZIDE may have potential as a building block in the synthesis of bioactive compounds and pharmaceuticals due to its unique structure and reactivity. It could also be used as a precursor in the development of new drugs or as a research tool in the exploration of new chemical reactions and mechanisms. Overall, 2-Methyl-quinoline-4-carboxylic acid hydrazide has potential in various areas of chemical and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 29620-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,2 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29620-66:
(7*2)+(6*9)+(5*6)+(4*2)+(3*0)+(2*6)+(1*6)=124
124 % 10 = 4
So 29620-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3O/c1-7-6-9(11(15)14-12)8-4-2-3-5-10(8)13-7/h2-6H,12H2,1H3,(H,14,15)
29620-66-4Relevant articles and documents
A highly selective fluorescent probe for Al3+ based on quinoline derivative
Wang, Guan-Qun,Qin, Jin-Can,Li, Chao-Rui,Yang, Zheng-Yin
, p. 21 - 25 (2015)
Abstract A novel Schiff base fluorescent probe, 1-phenyl-3-methyl-5-hydroxypyrazole-4-carbaldehyde (2′-methylquinoline-4′-formyl) hydrazone (PMHCH), for selective detection of Al3+ has been designed and synthesized. Upon addition of various met
Fluorescent sensor for selective detection of Al3+ based on quinoline-coumarin conjugate
Qin, Jing-Can,Li, Tian-Rong,Wang, Bao-Dui,Yang, Zheng-Yin,Fan, Long
, p. 38 - 43 (2014/07/07)
A fluorescence probe, 8-formyl-7-hydroxyl-4-methyl coumarin - (2′-methylquinoline-4-formyl) hydrazone (L) has been synthesized. The chemosensor is found preferential binding to Al3+ in presence of other competitive ions with associated changes in its optical and fluorescence spectra behavior. Upon addition of Al3+ to a solution of L, it shows 200-fold enhancement of fluorescence intensity which might be attributed to form a 2:1 stoichiometry of the binding mode of LAl(III) and the chelation enhanced fluorescence (CHEF) process at 479 nm in ethanol. The lowest detection limit for Al3+ is determined as 8.2 × 10-7 M.
