111265-51-1 Usage
Molecular structure
Bicyclic, containing a diazabicyclo ring and a carboxamide group
Stereochemistry
1S, 1α, 5α, and 6α configurations
Functional groups
Diazabicyclo ring, carboxamide, and N-methyl groups
Role
Used as a catalyst in various chemical reactions
Applications
a. Formation of urethanes
b. Synthesis of organic compounds
c. Potential use in pharmaceuticals and materials science
Advantages
a. Facilitates reactions under mild conditions
b. Versatility in catalyzing a variety of reactions
Importance
Valuable compound in the field of organic chemistry due to its efficiency and versatility in catalyzing chemical reactions
Check Digit Verification of cas no
The CAS Registry Mumber 111265-51-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,2,6 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111265-51:
(8*1)+(7*1)+(6*1)+(5*2)+(4*6)+(3*5)+(2*5)+(1*1)=81
81 % 10 = 1
So 111265-51-1 is a valid CAS Registry Number.
111265-51-1Relevant articles and documents
ASYMMETRICAL NITROGEN. 51. SYNTHESIS AND OPTICAL ACTIVATION OF 1,6-DIAZABICYCLOHEXANE-5-CARBOXYLIC ACID AND ITS DERIVATIVES
Shustov, G. V.,Denisenko, S. N.,Zolotoi, A. B.,D'yachenko, O. A.,Atovmyan, L. O.,Kostyanovskii, R. G.
, p. 2071 - 2076 (2007/10/02)
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1,2-Acyl Migration to an Electron-deficient Nitrogen Atom: a New Rearrangement of Diaziridines without Ring Opening
Denisenko, Sergei N.,Shustov, Gennady V.,Kostyanovsky, Remir G.
, p. 1275 - 1276 (2007/10/02)
5-Acyl-1,6-diazabicyclohexane (1) on treatment with t-butyl hypochlorite affords the corresponding N-chloro-derivative (2) which rearranges easily into 6-acyl-5-chloro-1,6-diazabicyclohexane (3) with a 1,2-shift of the acyl group.
