1150-40-9 Usage
General Description
2,4-dimethoxy-1,3,5-trinitrobenzene, also known as dinitroanisole (DNAN), is a synthetic organic compound with the chemical formula C8H6N2O6. It is a powerful explosive and is often used in military and industrial applications. DNAN is a yellow crystalline solid and is relatively insensitive to impact or friction, making it a safer alternative to other explosives. It has a high detonation velocity and energy yield, and is often used in combination with other explosives to enhance their performance. DNAN is also being investigated for its potential use in propellants, pyrotechnics, and other industrial applications. However, its production and handling must be carefully managed due to its explosive nature.
Check Digit Verification of cas no
The CAS Registry Mumber 1150-40-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1150-40:
(6*1)+(5*1)+(4*5)+(3*0)+(2*4)+(1*0)=39
39 % 10 = 9
So 1150-40-9 is a valid CAS Registry Number.
1150-40-9Relevant articles and documents
A mild one-pot procedure for the polynitration of activated arenes. Convenient preparation of dinitro- and trinitrodialkoxybenzenes
Nose,Suzuki
, p. 1539 - 1542 (2007/10/03)
When first treated with an excess of nitrogen dioxide alone and then in the presence of ozone at low temperature, dialkoxybenzenes are smoothly and stepwise polynitrated in a one-pot manner to afford the corresponding dinitro or trinitro derivatives in good yield.
An Unusual O-Methylation in the Allan-Robinson Synthesis of Purpurascenin, a 3,5,6,7,8,2',4',5'-Octamethoxyflavone
Patwardhan, Sarita A.,Gupta, Amrit S.
, p. 3786 - 3795 (2007/10/02)
In the Allan-Robinson synthesis of 3,5,6,7,8,2',4',5'-octamethoxyflavone (Purpurascenin, I), from 2,4,6-trihydroxy-3,5,ω-trimethoxyacetophenone (IV) and asarylic anhydride, the expected intermediate, 5,7-dihydroxy-3,6,8,2',4',5'-hexamethoxyflavone (III) unusually gets further methylated to give 5-hydroxy-3,6,7,8,2',4',5'-heptamethoxyflavone (II) during the course of reaction.The possible mechanism of methylation is discussed.
