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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.

598-92-5

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598-92-5 Usage

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

598-92-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-1-nitroethane

1.2 Other means of identification

Product number -
Other names Ethane, 1-chloro-1-nitro-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:598-92-5 SDS

598-92-5Upstream product

598-92-5Relevant academic research and scientific papers

Visible Light-Induced Oxidative Chlorination of Alkyl sp3 C-H Bonds with NaCl/Oxone at Room Temperature

Zhao, Mengdi,Lu, Wenjun

supporting information, p. 4560 - 4563 (2017/09/11)

A visible light-induced monochlorination of cyclohexane with sodium chloride (5:1) has been successfully accomplished to afford chlorocyclohexane in excellent yield by using Oxone as the oxidant in H2O/CF3CH2OH at room temperature. Other secondary and primary alkyl sp3 C-H bonds of cycloalkanes and functional branch/linear alkanes can also be chlorinated, respectively, under similar conditions. The selection of a suitable organic solvent is crucial in these efficient radical chlorinations of alkanes in two-phase solutions. It is studied further by the achievement of high chemoselectivity in the chlorination of the benzyl sp3 C-H bond or the aryl sp2 C-H bond of toluene.

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.

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