24006-87-9 Usage
Derivative of benzenediacetonitrile
Yes
Explanation
1,2-Benzenediacetonitrile,4,5-dimethylis a derivative of benzenediacetonitrile, which means it is structurally similar but has additional functional groups or modifications.
Explanation
The compound has two methyl (CH3) groups attached to the benzene ring at the 4th and 5th positions, which differentiates it from the parent compound.
Explanation
The compound is used as a starting material for the synthesis of various organic compounds, including those used in the pharmaceutical and agrochemical industries. It also serves as a solvent and intermediate in chemical reactions.
Explanation
1,2-Benzenediacetonitrile,4,5-dimethylhas been found to exhibit potential biological activities, such as fighting against microorganisms (antimicrobial) and inhibiting the growth of cancer cells (anticancer).
Explanation
The compound has diverse applications across these fields, including the synthesis of new compounds, development of pharmaceuticals, and understanding biological processes.
Methyl groups
Two at positions 4 and 5
Applications
Building block in organic synthesis, pharmaceuticals, agrochemicals, solvent, and intermediate in chemical reactions
Biological activities
Antimicrobial and anticancer properties
Fields of application
Chemistry, pharmaceuticals, and biochemistry
Check Digit Verification of cas no
The CAS Registry Mumber 24006-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,0 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24006-87:
(7*2)+(6*4)+(5*0)+(4*0)+(3*6)+(2*8)+(1*7)=79
79 % 10 = 9
So 24006-87-9 is a valid CAS Registry Number.
24006-87-9Relevant academic research and scientific papers
Process for the manufacture of 1,4-disubstituted bicyclic or tricyclic compounds and new 1,4-disubstituted bicyclic compounds
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, (2015/05/06)
The present invention provides a new process for the manufacture of 1,4-disubstituted bicyclic or tricyclic compounds by reacting a 1,2-bis-cyanomethyl-benzene or 2,3-bis-cyanomethyl-naphthalene with glyoxal in the presence of a base and a solvent as well as new 1,4-disubstituted bicyclic compounds.
