91346-98-4 Usage
Description
1,10-Dinitrodecane is a chemical compound characterized by the molecular formula C10H20N2O4. It is a nitroalkane that features two nitro functional groups attached to a 10-carbon chain. 1,10-Dinitrodecane is known for its highly flammable and explosive properties, which necessitates careful handling, storage, and adherence to safety guidelines and regulations to mitigate risks to human health and the environment.
Uses
Used in Explosives Production:
1,10-Dinitrodecane is utilized as a key component in the production of explosives due to its high flammability and explosive nature. Its properties make it a valuable asset in the creation of powerful explosive materials for various applications.
Used as a Chemical Intermediate:
In the chemical industry, 1,10-Dinitrodecane serves as an important intermediate in the synthesis of other organic compounds. Its unique structure and reactivity allow it to be a building block for the development of a range of chemical products, contributing to the diversity of chemical manufacturing processes.
Check Digit Verification of cas no
The CAS Registry Mumber 91346-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,4 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91346-98:
(7*9)+(6*1)+(5*3)+(4*4)+(3*6)+(2*9)+(1*8)=144
144 % 10 = 4
So 91346-98-4 is a valid CAS Registry Number.
91346-98-4Relevant articles and documents
Oxidation of azides by the HOF·CH3CN: A novel synthesis of nitro compounds
Carmeli, Mira,Rozen, Shlomo
, p. 4585 - 4589 (2007/10/03)
The HOF·CH3CN complex, readily prepared by passing F 2 through aqueous acetonitrile, is an exceptionally efficient oxygen transfer agent. It is unique in its capacity to oxidize various azides into the corresponding nitro derivatives. This method requires short reactions times and room temperature or below, and the desired nitro compounds were usually isolated in very good yields. The respective nitroso derivatives are believed to be the intermediates in this reaction. Functional groups such as aromatic rings, ketones, nitriles, halides, alcohols, and esters are tolerated. Sulfides react with HOF·CH3CN usually at the same rate as azides. Amines and olefins, however, react faster, so they have to be protected first. Nitro derivatives with various oxygen isotopes can be made using the labeled H 18OF·CH3CN. In the case of chiral azides the stereochemistry around the nitrogen-bonded carbons is retained.