13591-65-6 Usage
Structure
Bicyclic organic compound with a diazabicyclic ring system
Substituents
Dimethyl (CH3)2
4-Nitrophenyl (C6H4(NO2)-4)
Phenyl (C6H5)
Configuration
cis(substituents on the same side of the ring structure)
Potential Applications
Organic synthesis
Catalysis
Pharmaceutical research
Hazards
Potential hazards and reactivity due to its complex structure
Handling
Use caution when handling and working with 1,3-Diazabicyclo[3.1.0]hex-3-ene,
2,2-dimethyl-6-(4-nitrophenyl)-4-phenyl-, cis-
Stability
May be sensitive to heat, light, or moisture
Solubility
Soluble in organic solvents such as dichloromethane, acetone, or ethanol
Melting Point
Not provided in the material, but can be determined experimentally
Boiling Point
Not provided in the material, but can be determined experimentally
Density
Not provided in the material, but can be determined experimentally
Optical Activity
May exhibit optical isomerism due to the presence of a chiral center
Reactivity
May react with nucleophiles, electrophiles, or other reactive species depending on the reaction conditions
Synthesis
Can be synthesized through various methods, such as cyclization reactions or condensation reactions involving the corresponding precursors
Purity
The purity of the compound can be determined using techniques like chromatography or spectroscopy
Safety Measures
Use appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats when handling 1,3-Diazabicyclo[3.1.0]hex-3-ene,
2,2-dimethyl-6-(4-nitrophenyl)-4-phenyl-, cis-
Disposal
Dispose of the compound according to local regulations and guidelines for hazardous materials
Environmental Impact
Potential environmental impact if not handled and disposed of properly, due to its complex structure and reactivity
Check Digit Verification of cas no
The CAS Registry Mumber 13591-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,9 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13591-65:
(7*1)+(6*3)+(5*5)+(4*9)+(3*1)+(2*6)+(1*5)=106
106 % 10 = 6
So 13591-65-6 is a valid CAS Registry Number.
13591-65-6Relevant academic research and scientific papers
Mahmoodi,Kiyani,Tabatabaeian,Zanjanchi,Arvand,Sharifzadeh
, p. 884 - 889 (2010)
Several 6-(4-nitrophenyl)-4-phenyl-1,3-diazabicyclo[3.1.0]hex-3-ene derivatives having various substituents on C2 were synthesized, and their 1H NMR spectra and photochromic behavior were examined.
Two 1,3-Diazabicyclo[3.1.0]hex-3-enes with a 'Tripod' core
Mahmoodi, Nosrat O.,Tabatabaeian, Khalil,Kiyani, Hamzeh
experimental part, p. 536 - 542 (2012/05/04)
The photochromic 1,3-diazabiclyclo[3.1.0]hex-3-enes 5 and 6 were synthesized from two premade tris-aldehydes and two premade aziridinyl ketones and characterized (Scheme 1). Their spectra showed structurei-photochromic behavior relationships (SPBR), which were analyzed. Copyright
AZIRIDINYL KETONES AND THEIR CYCLIC ANILS. 9. SUBSTITUTED 1,3-DIAZABICYCLOHEX-3-ENES
Kaluski, Z.,Gresyak-Figas, A.,Vorob'eva, N. P.,Bakumenko, A. I.,Yaremenko, F. G.,Orlov, V. D.
, p. 888 - 893 (2007/10/02)
Aryl-substituted 1,3-diazabicyclohex-3-enes were obtained by the reaction of α,β-dibromodihydrochalcones with ammonia and formaldehyde (or acetone).Their strucures were confirmed by spectral methods and x-ray diffraction analysis.
