598-92-5 Usage
Description
1-Chloro-1-nitroethane, also known as nitroethyl chloride, is a chemical compound with the molecular formula C2H4ClNO2. It is a pale yellow liquid with a sharp, unpleasant odor and is mainly used in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is also employed as a solvent and a starting material for the production of other compounds. However, it is considered a hazardous material due to its toxicity if swallowed or inhaled, potential to cause skin and eye irritation upon contact, and its flammability.
Uses
Used in Pharmaceutical Industry:
1-Chloro-1-nitroethane is used as a key intermediate in the synthesis of various pharmaceutical compounds for its versatile reactivity and ability to be converted into a wide range of products.
Used in Agrochemical Industry:
1-Chloro-1-nitroethane is used as a starting material in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used as a Solvent:
1-Chloro-1-nitroethane is used as a solvent in various chemical processes, taking advantage of its ability to dissolve a range of substances and facilitate reactions.
Used in Production of Other Compounds:
1-Chloro-1-nitroethane serves as a starting material for the synthesis of other chemical compounds, highlighting its importance in the broader field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 598-92-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 598-92:
(5*5)+(4*9)+(3*8)+(2*9)+(1*2)=105
105 % 10 = 5
So 598-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C2H4ClNO2/c1-2(3)4(5)6/h2H,1H3
598-92-5Relevant articles and documents
Levering
, p. 2930 (1962)
Electrooxidative coupling of salts of nitro compounds with halide, nitrite, cyanide, and phenylsulfinate anions
Ilovaisky,Merkulova,Ogibin,Nikishin
, p. 1585 - 1592 (2007/10/03)
Electrolysis of salts of primary and secondary nitro compounds (nitroethane, 1- and 2-nitropropanes, nitrocyclohexane, and nitrocycloheptane) in the presence of excess halide, nitrite, cyanide, and phenylsulfinate anions under undivided and divided amperostatic electrolysis conditions in a two-phase medium (CH2Cl2/H2O) produces geminal nitrohalides (35-85% yields), dinitro compounds (15-51%), nitronitriles (6-27%), and nitrosulfones (50-70%). The salts of secondary nitro compounds form the products of oxidative coupling with halide and phenylsulfinate anions under the undivided electrolysis conditions. In all other cases, divided electrolysis is required.
