762-98-1 Usage
Uses
Used in Military Applications:
2,2-DIMETHYL-1,3-DINITROPROPANE is used as a high-energy explosive for its capacity to deliver a powerful blast in military operations. Its high-velocity characteristics are particularly valuable for applications requiring a rapid and forceful impact.
Used in Industrial Applications:
In the industrial sector, 2,2-DIMETHYL-1,3-DINITROPROPANE is utilized as a component in the synthesis of other explosives, capitalizing on its high energy density to enhance the performance of these compounds.
Used in Research and Development:
2,2-DIMETHYL-1,3-DINITROPROPANE is employed as a subject of study in research and development for new explosive formulations, aiming to improve the safety, stability, and efficiency of explosive materials.
However, due to its extreme volatility and sensitivity to heat, shock, and friction, 2,2-DIMETHYL-1,3-DINITROPROPANE is a restricted chemical in many countries, necessitating strict regulations and careful handling to mitigate the risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 762-98-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 762-98:
(5*7)+(4*6)+(3*2)+(2*9)+(1*8)=91
91 % 10 = 1
So 762-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2O4/c1-5(2,3-6(8)9)4-7(10)11/h3-4H2,1-2H3
762-98-1Relevant articles and documents
P(RNCH2CH2)3N: An Efficient Promoter for the Nitroaldol (Henry) Reaction
Kisanga, Philip B.,Verkade, John G.
, p. 4298 - 4303 (2007/10/03)
The use of catalytic amounts of the proazaphosphatranes P(MeNCH2CH2)3N, P(i-PrNCH2CH2)3N and P(HNCH2CH2)(i-PrNCH2CH2) 2N as nonionic bases in the reaction of nitroalkanes with carbonyl compounds is reported. The reaction proceeds at room temperature in the presence of 2.2 equiv of magnesium sulfate to produce the corresponding β-nitroalkanols in generally superior yields. Aldehydes react quantitatively in 5-60 min, whereas ketones require up to 3 h to react with nitromethane and up to 7 h for the reaction of ketones with higher nitroalkanes.
