92487-36-0 Usage
Description
(3Z)-3-[(2,2-dimethylhydrazino)methylidene]-3H-indole is a chemical compound with the molecular formula C11H14N4. It is a derivative of indole and contains a hydrazine group. (3Z)-3-[(2,2-dimethylhydrazino)methylidene]-3H-indole is a potential candidate for pharmaceutical research due to its unique structure and potential medicinal properties.
Uses
Used in Pharmaceutical Research:
(3Z)-3-[(2,2-dimethylhydrazino)methylidene]-3H-indole is used as a potential candidate for pharmaceutical research for its unique structure and potential medicinal properties. It may have applications in the development of drugs targeting certain biological pathways or receptors.
Further research is needed to fully understand the potential uses and effects of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 92487-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,8 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92487-36:
(7*9)+(6*2)+(5*4)+(4*8)+(3*7)+(2*3)+(1*6)=160
160 % 10 = 0
So 92487-36-0 is a valid CAS Registry Number.
92487-36-0Relevant articles and documents
Lewis Acid Catalyzed Reactions of α,β-Unsaturated N,N-Dimethylhydrazones with 1,4-Benzoquinone. Formation of Indoles by a Novel Oxidative Rearrangement
Echavarren, Antonio M.
, p. 4255 - 4260 (2007/10/02)
The Diels-Alder reaction of quinones and (E)-3-arylpropenal N,N-dimethylhydrazones only proceeds with 1,4-naphthoquinone as the dienophile.The addition of Lewis acids leads to the formation of trans-2,3-dihydrobenzofurans in a highly regioselective process.When propenal N,N-dimethylhydrazones 4 and 5 were allowed to react with 1,4-benzoquinone and boron trifluoride, an unprecedented oxidative rearrangement took place yielding indole-3-carboxaldehyde N,N-dimethylhydrazones 7 and 8, respectively.
Potential anticonvulsants. VIII. Some hydrazones of indole-3-carboxaldehyde
Popp
, p. 617 - 619 (2007/10/02)
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