Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Chloromethyl methyl ether (CMME) is a compound with formula CH3OCH2Cl. A colorless liquid, it is a chloroalkyl ether. It is used as an alkylating agent. In organic synthesis, it is used for introducing the methoxymethyl ether (MOM) protecting group,[3] and is thus often called MOM-Cl or MOM chloride. It also finds application as a chloromethylating agent in some variants of the Blanc chloromethylation.[4]
^Sigma-Aldrich
^ abcdeNIOSH Pocket Guide to Chemical Hazards. "#0129". National Institute for Occupational Safety and Health (NIOSH).
^Protective Groups in Organic Synthesis, T. W. Greene and P. G. M. Green, 3rd Edition, pages 27-33. ISBN 0-471-16019-9
^Wuts, Peter G. M. (2001). "Chloromethyl Methyl Ether". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rc118. ISBN 0471936235.
and 24 Related for: Chloromethyl methyl ether information
Chloromethylmethylether (CMME) is a compound with formula CH3OCH2Cl. A colorless liquid, it is a chloroalkyl ether. It is used as an alkylating agent...
dichloromethane or chloroform. This method is preferred to the use of chloromethylmethylether (MOMCl). Phenols can also be MOM-protected using dimethoxymethane...
range of Lewis and Bronsted acids. Chloromethylmethylether and chloromethoxyethoxymethane, like other chloroalkyl ethers, are strong alkylating agents with...
better results under modified chloromethylation conditions using chloromethylmethylether (MOMCl) in the presence of 60% H2SO4. Highly activated arenes...
from triphenylphosphine. The first step is P-alkylation with chloromethylmethylether. PPh3 + CH3OCH2Cl → [CH3OCH2PPh3]Cl In the second step, the resulting...
connected to a chloromethyl group via an alkane chain. Chloromethylmethylether (CMME) is an ether with the formula CH3OCH2Cl. It is used as an alkylating...
and triazoles. Tertiary amines can react with DCM to form quaternary chloromethyl chloride salts via the Menshutkin reaction. Secondary amines can react...
For all listings above which contain the word "compounds" and for glycol ethers, the following applies: Unless otherwise specified, these listings are defined...
mass: 80.0029 u) may refer to: 1-Chloroethanol 2-Chloroethanol Chloromethylmethylether (CMME) Ethyl hypochlorite This set index page lists chemical structure...
Eterobarb can be synthesized by reacting phenobarbital with chloromethylmethylether in presence of a base. Gallagher BB, Baumel IP, Woodbury SG, Dimicco...
When conducted in the presence of hydrogen chloride, the product is the chloromethyl compound, as described in the Blanc chloromethylation. If the arene is...
The same year they also described a «polysilicic acid ether» in the preparation of ethyl- and methyl-o-silicic acid. Extensive research in the field of organosilicon...
chlorinating agents such as sulfuryl chloride, dimethyl sulfide converts to chloromethylmethyl sulfide: SO2Cl2 + (CH3)2S → SO2 + HCl + ClCH2SCH3 Like other methylthio...
96 g/mol, exact mass: 113.9639 u) may refer to: Bis(chloromethyl) ether Dichloromethyl methylether This set index page lists chemical structure articles...
fluids and tissues of a man who died one week post-exposure. Bis(chloromethyl) ether Chlorine gas Keen as Mustard Phosgene oxime Poison gas in World War...
No. no longer in use) UN 1237 3 Methyl butyrate UN 1238 6.1 Methyl chloroformate UN 1239 6.1 Methylchloromethylether UN 1240 to 1241 ? (UN No.s no longer...
the original on 12 October 2007. White, E.P. 1954. “The occurrence of N-methyl-β-phenylethylamine in Acacia prominens A. Cunn.” New Zealand J. Sci. & Tech...
cyclic ether. Needed chemistry was observed and developed through the 1930s and 1940s. The very first polymerized oxetane was 3,3-bis(chloromethyl)oxetane...