6307-92-2 Usage
Molecular structure
A benzene ring with a phenylethenyl group attached to the 2nd carbon, and nitro groups (-NO2) attached to the 1st, 3rd, and 5th carbons.
Appearance
Yellow crystalline solid
Explosive properties
Highly explosive and sensitive to friction, heat, and shock
Applications
a. Production of explosives
b. Propellants
c. Pyrotechnics
Advantages
a. High energy content
b. Stability
c. Attracts use in military and industrial applications
Environmental impact
Potent environmental pollutant
Health concerns
Harmful effects on human health
Ongoing efforts
Development of safer alternatives in explosive materials
Check Digit Verification of cas no
The CAS Registry Mumber 6307-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6307-92:
(6*6)+(5*3)+(4*0)+(3*7)+(2*9)+(1*2)=92
92 % 10 = 2
So 6307-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H9N3O6/c18-15(19)11-8-13(16(20)21)12(14(9-11)17(22)23)7-6-10-4-2-1-3-5-10/h1-9H
6307-92-2Relevant articles and documents
Efficient Palladium(0) supported on reduced graphene oxide for selective oxidation of olefins using graphene oxide as a ‘solid weak acid’
Gao, Xi,Zhou, Jianhao,Peng, Xinhua
, p. 73 - 78 (2019/02/06)
Selective oxidation of olefin derivatives to ketones has made innovative development over palladium(0) supported on reduced graphene oxide. Compared to traditional Wacker oxidation, the novel method offers an economical and environment-friendly option by using graphene oxide (GO) as a ‘solid weak acid’ instead of classical homogeneous catalysts like H2SO4 and CF3COOH. X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscope and transmission electron microscopy images of Pd0/RGO showed that the nanoscaled Pd particles generated at the flake structure of reduced graphene oxide. Under optimized condition, up to 44 kinds of ketones with different structures can be prepared with excellent yields.
