120340-35-4 Usage
Structure
Ester derivative of 1,4-Diazabicyclo[2.2.2]octane-2-methanol
Functional Groups
Ester, Amine
Type of Compound
Organic compound
Application
a. Catalyst in various organic reactions
b. Base in the synthesis of pharmaceuticals and agrochemicals
c. Curing agent for epoxy resins
Reactivity
High reactivity and selectivity
Importance
Important tool in the field of organic chemistry
Safety Precautions
Handle with caution due to potential health risks
Check Digit Verification of cas no
The CAS Registry Mumber 120340-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,4 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120340-35:
(8*1)+(7*2)+(6*0)+(5*3)+(4*4)+(3*0)+(2*3)+(1*5)=64
64 % 10 = 4
So 120340-35-4 is a valid CAS Registry Number.
120340-35-4Relevant articles and documents
Diazabicycloalkanes with nitrogen atoms in the nodal positions. 5. Synthesis and some reactions of 2-hydroxymethyl-1,4-diazabicyclo [2.2.2]octane
Shishkin,Vysochin
, p. 1069 - 1072 (1981)
2-Hydroxymethyl-1,4-diazabicyclo[2.2.2]octane was synthesized by reduction of 1,4-diazabicyclo[2.2.2]octane-2-carboxylic acid or its methyl ester with lithium aluminum hydride in tetrahydrofuran and by hydrolysis or hydrogenation of 2-benzyloxymethyl-1,4-diazabicyclo[2.2.2]octane. Depending on the conditions, 2-hydroxymethyl-1,4-diazabicyclo[2.2.2]octane reacts with methyl iodide to give primarily either a bisquaternary or a monoquaternary derivative. The latter is the only product in its alkylation with methyl esters of benzoic and caproic acids.
