6969-11-5 Usage
Chemical compound
A substance formed by a chemical reaction, consisting of a specific arrangement of atoms.
Nitrogen-containing heterocyclic ring structure
A ring-shaped structure containing nitrogen atoms, which contributes to the compound's reactivity and potential applications.
Quaternary ammonium salt
A type of salt derived from an ammonium ion (NH4+) in which all four hydrogen atoms are replaced by organic groups, giving the compound a positive charge.
Cyano group
A functional group with the formula CN, consisting of a carbon atom triple-bonded to a nitrogen atom, which can act as a nucleophile or electrophile in chemical reactions.
Carbonyl group
A functional group with the formula C=O, consisting of a carbon atom double-bonded to an oxygen atom, which can participate in various reactions, such as nucleophilic addition and electrophilic substitution.
Reactivity
The compound's ability to undergo chemical reactions, making it useful in the synthesis of pharmaceuticals and other organic compounds.
Building block
A component that can be used to construct more complex molecules, which is valuable in the development of new drugs or materials.
Organic chemistry applications
The compound's unique structure and reactivity make it a valuable reagent or intermediate in multi-step synthesis processes.
Potential for new drug development
The compound's properties and reactivity may hold promise for the development of new drugs or materials, contributing to advancements in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6969-11-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6969-11:
(6*6)+(5*9)+(4*6)+(3*9)+(2*1)+(1*1)=135
135 % 10 = 5
So 6969-11-5 is a valid CAS Registry Number.
6969-11-5Relevant articles and documents
Synthesis and nucleophilic reactions of cyano substituted N-methoxyisoquinolinium salts
Heber,Holzgrabe,Werra
, p. 785 - 790 (2007/10/02)
Starting from isoquinoline, the cyano substituted N-methoxyisoquinolinium salts 1.1 and 1.4 are prepared. Their behaviour in the presence of O-, C- and N-nucleophiles in different aprotic solvents is examined: from the 1-cyano substituted isoquinolinium derivative 1.1, 1- and 3-aminals or 1-iminium salts are obtained depending on the amine used, and N-methoxyisocarbostyril 4.1.1 in H2O and OH-. The reaction of the 4-cyano-N-methoxyisoquinolinium salt 1.4 with amines yields 1-aminals and with OH- the corresponding hemiaminal. Conversion with CN- results in dinitrile derivatives and N-oxides.
