301315-87-7 Usage
Chemical Structure
It contains a pyrimidinedione ring with an amino group (NH2) attached to the 2-position and a nitro group (NO2) attached to the 5-position.
Reactivity
Highly reactive and potentially explosive due to the presence of the nitro group.
Applications
Manufacture of Explosives: Its explosive properties make it useful in the production of explosives.
Dyes Production: Used in the manufacturing process of dyes.
Pharmaceuticals: Employed in pharmaceutical synthesis.
Functional Groups
Nitro Group (NO2): Responsible for its explosive properties.
Amino Group (NH2): Enables participation in various chemical reactions.
Usage Fields
Organic Chemistry: Used as a reagent in various organic synthesis processes.
Pharmaceuticals: Utilized in the synthesis of pharmaceutical compounds.
Military Explosives: Applied in the production of explosives for military use.
Handling
Requires careful handling due to its potential instability and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 301315-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,3,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 301315-87:
(8*3)+(7*0)+(6*1)+(5*3)+(4*1)+(3*5)+(2*8)+(1*7)=87
87 % 10 = 7
So 301315-87-7 is a valid CAS Registry Number.
301315-87-7Relevant articles and documents
Diaminomethyleneaminocarbonyldinitromethane, formed during the preparation of 2-amino-6-chloro-5-nitro-4(3H)-pyrimidinone by nitration of 2-amino-6-chloro-4(3H)-pyrimidinone
Boyle, Peter H.,Daly, Karen M.,Leurquin, Fabien,Robinson, J. Kenneth,Scully, Damien T.
, p. 1793 - 1795 (2007/10/03)
Difficulties in the nitration of 2-amino-6-chloro-4(3H)-pyrimidinone to give the widely used heterocyclic precursor 2-amino-6-chloro-5-nitro-4(3H)-pyrimidinone are shown to be due to formation of an unusual open-chain gem-dinitro compound, identified as diaminomethyleneaminocarbonyldinitromethane. The latter is also formed by the nitration of 2-amino-4,6(3H,5H)-pyrimidinedione. It decomposes with loss of carbon dioxide in dimethyl sulfoxide, or in aqueous potassium hydroxide, to give guanidine and dinitromethane.
