62908-29-6 Usage
Uses
Used in Pharmaceutical Industry:
(6E)-6-[2-(4-nitrophenyl)hydrazinylidene]hexane-1,2,3,4,5-pentol (non-preferred name) is used as a potential pharmaceutical compound for its hydrazine and nitrophenyl groups, which may contribute to its activity against certain diseases or conditions. The presence of multiple hydroxyl groups could also facilitate interactions with biological targets.
Used in Organic Synthesis:
In the field of organic synthesis, (6E)-6-[2-(4-nitrophenyl)hydrazinylidene]hexane-1,2,3,4,5-pentol (non-preferred name) can be used as a building block or intermediate for the synthesis of more complex molecules. Its structural features, including the hydrazinylidene and nitrophenyl moieties, may allow for further functionalization and the creation of novel compounds.
Used as a Reagent in Chemical Reactions:
(6E)-6-[2-(4-nitrophenyl)hydrazinylidene]hexane-1,2,3,4,5-pentol (non-preferred name) may serve as a reagent in various chemical reactions due to its reactive functional groups. The nitro group, for instance, can be reduced or used in other reactions, while the hydrazinylidene group could participate in condensation or coupling reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 62908-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,0 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62908-29:
(7*6)+(6*2)+(5*9)+(4*0)+(3*8)+(2*2)+(1*9)=136
136 % 10 = 6
So 62908-29-6 is a valid CAS Registry Number.
62908-29-6Relevant academic research and scientific papers
Hydrogen-Bonding Network Anchors the Cyclic Form of Sugar Arylhydrazones
Goldschmidt G?z, Viktória,Pintér, István,Csámpai, Antal,Jákli, Imre,Zsoldos-Mády, Virág,Perczel, András
supporting information, p. 3419 - 3426 (2016/07/23)
The “classical” challenge, raised by Emil Fischer as to why one monosaccharide arylhydrazone adopts a cyclic structure but another an acyclic structure, is answered here. The present comprehensive analysis of hexose and hexosamine arylhydrazones, based on 2D NMR spectroscopy and theoretical modeling, has established that the chain of hydrogen bonds needed for conformational selection can only be completed for d-glucosamine derivatives. Thus, d-glucosamine 4-nitrophenylhydrazone exclusively adopts its cyclic form, but any configurational changes imply the formation of acyclic structures. In conclusion, three criteria dominate structure selection, namely 1) an amino function at the C-2 position, 2) the “all-equatorial” substitution mode of the pyranoid ring, and 3) an electron-withdrawing group on the arylhydrazone are all needed to get the cyclic form only.
