55402-83-0 Usage
Uses
Used in Chemical Synthesis:
3,6-DIAZABICYCLO[3.2.0]HEPTANE is used as a catalyst and a base for various chemical reactions, particularly in organic synthesis. Its high basicity and nucleophilicity make it an effective reagent in a variety of chemical transformations.
Used in Formation of Carbon-Carbon Bonds:
In the Chemical Synthesis Industry, 3,6-DIAZABICYCLO[3.2.0]HEPTANE is used as a catalyst and a base for the formation of carbon-carbon bonds, which are essential in creating complex organic molecules.
Used in Deprotonation of Acidic Compounds:
In the Chemical Synthesis Industry, 3,6-DIAZABICYCLO[3.2.0]HEPTANE is used as a catalyst and a base for the deprotonation of acidic compounds, facilitating the formation of new chemical species.
Used as a Ligand in Coordination Chemistry:
3,6-DIAZABICYCLO[3.2.0]HEPTANE has applications as a ligand in coordination chemistry, where it can form complexes with metal ions, contributing to the development of new materials and catalysts.
Used as a Phase-Transfer Catalyst in Organic Reactions:
In the Organic Synthesis Industry, 3,6-DIAZABICYCLO[3.2.0]HEPTANE is used as a phase-transfer catalyst to facilitate reactions between organic and inorganic compounds, enhancing the efficiency and selectivity of various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 55402-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,0 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55402-83:
(7*5)+(6*5)+(5*4)+(4*0)+(3*2)+(2*8)+(1*3)=110
110 % 10 = 0
So 55402-83-0 is a valid CAS Registry Number.
55402-83-0Relevant academic research and scientific papers
Synthesis of a new bridged diamine 3,6-diazabicyclo [3.2.0] heptane: Applications to the synthesis of quinolone antibacterials
Jacquet,Bouzard,Kiechel,Remuzon
, p. 1565 - 1568 (2007/10/02)
Diprotected 3,6-diazabicyclo [3.2.0] heptane has been prepared by an highly efficient process. Selective deprotection, followed by condensation with 7-halogenoquinolones led to the naphthyridones 10 and 13 and the quinolone 14.
