918-52-5 Usage
Description
2,2-Dinitropropanol, with the molecular formula C3H7NO4, is a pale yellow solid chemical compound. It has a molecular weight of 133.10 g/mol and is known for its high reactivity. Due to its potential mutagenicity and carcinogenicity, it is considered a hazardous substance that can cause irritation to the skin, eyes, and respiratory system upon exposure. It requires careful handling in both laboratory and industrial environments.
Uses
Used in Pharmaceutical Industry:
2,2-Dinitropropanol is used as a precursor in the synthesis of various pharmaceuticals. Its reactivity allows for the creation of a range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Pesticide Industry:
In the pesticide industry, 2,2-Dinitropropanol serves as a starting material for the production of different types of pesticides. Its chemical properties make it suitable for the formulation of effective pest control agents.
Given the potential hazards associated with 2,2-Dinitropropanol, it is crucial to implement stringent safety measures during its use in both the pharmaceutical and pesticide industries to minimize health and environmental risks.
Check Digit Verification of cas no
The CAS Registry Mumber 918-52-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 918-52:
(5*9)+(4*1)+(3*8)+(2*5)+(1*2)=85
85 % 10 = 5
So 918-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H6N2O5/c1-3(2-6,4(7)8)5(9)10/h6H,2H2,1H3
918-52-5Relevant articles and documents
Catalyzed Oxidative Nitration of Nitronate Salts
Garver, Lee C.,Grakauskas, V.,Baum, Kurt
, p. 1699 - 1702 (2007/10/02)
Nitronate salts are converted to gem-dinitro compounds with nitrite ion and persulfate, in the presence of a catalytic amount of ferricyanide.The use of cyanide or sulfinate salts in place of nitrile gave gem-cyanonitro compounds and α-nitro sulfones, respectively.
