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2-Chloro-2-methyloctane, also known as 2-chloro-2-methyl-C8H18, is an organic compound with the molecular formula C9H19Cl. It is a colorless liquid with a density of 0.84 g/cm3 and a boiling point of 183-185°C. This chemical is primarily used as a solvent, a chemical intermediate in the synthesis of various compounds, and as a reagent in organic reactions. It is also employed in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its chlorinated nature, 2-chloro-2-methyloctane can be hazardous and requires proper handling and storage to prevent environmental and health risks.

928-60-9

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928-60-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 928-60-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 928-60:
(5*9)+(4*2)+(3*8)+(2*6)+(1*0)=89
89 % 10 = 9
So 928-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H19Cl/c1-4-5-6-7-8-9(2,3)10/h4-8H2,1-3H3

928-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CHLORO-2-METHYLOCTANE

1.2 Other means of identification

Product number -
Other names 2-Chlor-2-methyl-octan

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:928-60-9 SDS

928-60-9Relevant academic research and scientific papers

α,ω-Dialkyl-Substituted Polyenes by Palladium-Catalyzed Coupling Reactions of Vinyltin Compounds with Vinyl Halides

Kiehl, Alfried,Eberhardt, Anke,Muellen, Klaus

, p. 223 - 230 (2007/10/02)

α,ω-Dialkyl-substituted linear polyenes are synthesized in good yields by the palldium-catalyzed coupling reaction of trialkyltin- and iodo-substituted olefinic precursors.Central building blocks are the distannylated butadiene 8 and vinyl iodide 3.Our synthetic strategy was successfully applied to the preparation of the tert-butyl polyenes 13, 14, and 15 as well as polyenes 25 and 26 with longer α,ω-dialkyl chains. - Key Words: Polyenes, linear/ Vinyl tin compounds/ Vinyl halides/ Palladium catalysis

CHLORIERENDE METHYLIERUNG VON ALDEHYD- UND KETOGRUPPEN MIT NIOB-REAGENZIEN SOWIE AUFKLAERUNG DES MECHANISMUS

Kauffmann, Thomas,Abel, Thomas,Neiteler, Gabriele,Schreer, Martin

, p. 503 - 506 (2007/10/02)

The reagents MeNbCl4 and Me2NbCl3, applied as isolated pure compounds, react with ketones in preparatively useful yields according to RR'CO -> RR'C(Cl)CH3.Whereas benzaldehyde reacts with MeNbCl4 analogously, the aliphatic aldehyde heptanal forms beside the expected product two cinechlorination products, indicating a mechanism via radicals.MeNbCl4 is highly aldehyde-vs.-ketone selective.Conversely, high ketone-vs.-aldehyde selectivity is achievable by application of MeNbCl4*PPh3 or NbCl5*PPh3 + 1.5 Me2Zn.

REGIOSPECIFIC AND STEREOSPECIFIC SUBSTITUTION OF HYDROXYL IN ALIPHATIC ALCOHOLS BY HALOGEN

Matveeva, E. D.,Kurts, A. L.,Yalovskaya, A. I.,Nikishova, N. G.,Bundel', Yu. G.

, p. 642 - 646 (2007/10/02)

A new system containing triphenylphosphine and trichloro- and tribromoacetic ester makes it possible to substitute the hydroxyl group in alcohols by halogen.Regiospecific and stereospecific substitution of the hydroxyl by the halogen takes place as a result of the reaction of primary and secondary aliphatic alcohols and of 2-alkenols, susceptible to isomerization processes, with this system.

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