111265-53-3 Usage
Molecular Structure
Derived from 1,6-diazabicyclo[3.1.0]hexane The compound has a bicyclic structure with nitrogen atoms in the ring.
Functional Group
Carboxylic acid and ester groups The carboxylic acid group is present at the 5-position, and the ester group is formed by the methyl ester at the same position.
Stereochemistry
[1R-(1alpha,5alpha,6alpha)] The stereochemistry of the compound is defined by the configuration at the 1, 5, and 6 positions.
Application
Catalyst in organic synthesis The compound is used to facilitate various chemical reactions, including asymmetric transformations.
Versatility
Facilitates a variety of reactions The compound can be used in different types of organic reactions due to its unique structure.
Stability
High stability The compound can be used under a range of reaction conditions, making it a valuable tool in organic chemistry.
Field of Use
Organic chemistry The compound is particularly valuable for chemists and researchers working in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 111265-53-3 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 111265-53:
(8*1)+(7*1)+(6*1)+(5*2)+(4*6)+(3*5)+(2*5)+(1*3)=83
83 % 10 = 3
So 111265-53-3 is a valid CAS Registry Number.
111265-53-3Relevant articles and documents
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.
