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79-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79-24-3 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79-24:
63 % 10 = 3
So 79-24-3 is a valid CAS Registry Number.



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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017


1.1 GHS Product identifier

Product name nitroethane

1.2 Other means of identification

Product number -
Other names Nitroetan [Polish]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Fuels and fuel additives,Solvents (for cleaning or degreasing),Solvents (which become part of product formulation or mixture)
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:79-24-3 SDS

79-24-3Relevant articles and documents



, p. 24 (1944)


Formation of positive and negative ions in CH3NO2

Jiao,DeJoseph Jr.,Garscadden

, p. 9040 - 9044 (2003)

Absolute dissociative ionization cross-sections from threshold to 200 eV have been measured using Fourier transform mass spectrometry (FTMS). In the production of positive ions by electron impact ionization, 13 ions are detected, including the parent ion

IR Spectroscopy of the Gas Phase Formed after Interaction between CH3I and Ag-Containing Sorbents Based on Silica Gel

Krapukhin, V. B.,Kulyukhin, S. A.,Rumer, I. A.

, p. 465 - 470 (2020/04/17)

Abstract: IR spectra of the gas phase formed during the interaction between gaseous CH3I and SiO2-based granular sorbents containing various silver compounds are studied. It is established that the main gaseous products formed by the

Green synthesis of low-carbon chain nitroalkanes via a novel tandem reaction of ketones catalyzed by TS-1

Chu, Qingyan,He, Guangke,Xi, Yang,Wang, Ping,Yu, Haoxuan,Liu, Rui,Zhu, Hongjun

, p. 46 - 50 (2018/02/09)

A green and efficient one-pot method has been developed for the synthesis of low-carbon chain nitroalkanes via a novel TS-1 catalyzed tandem oxidation of ketones with H2O2 and NH3. The tandem reaction including ammoxidation, oximation and oxidation of oximes, afforded up to 88% yield and 98% chemo-selectivity requiring only 90 min, at 70 °C and atmospheric pressure. Moreover, this method was even amenable to 100-fold scale-up without loss of chemical efficiency with 87% yield, represents a significant advance towards industrial production of nitroalkanes. Furthermore, the plausible mechanism of TS-1 catalyzed tandem oxidation of ketones to prepare nitroalkanes was proposed.

S-alkylation of thiacalixarenes: A long-neglected possibility in the calixarene family

Kundrat, Ondrej,Eigner, Vaclav,Dvorakova, Hana,Lhotak, Pavel

supporting information; scheme or table, p. 4032 - 4035 (2011/09/20)

Despite the high nucleophilicity of sulfur atoms, thiacalixarenes have been alkylated only on oxygen atoms thus far. Using strong alkylating agents (triflates, trialkyloxonium salts), the substitution of the sulfur bridges has been successfully accomplished. The corresponding sulfonium salts of thiacalix[4]arene are formed regio- and stereoselectively as a completely new type of substitution pattern in thiacalixarene chemistry. These compounds possess interesting conformational behavior and could be used as unusual alkylating agents with uncommon selectivity.