Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H3ClO2 |
| Molecular Weight | 94.497 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(Cl)=O
InChI
InChIKey=XMJHPCRAQCTCFT-UHFFFAOYSA-N
InChI=1S/C2H3ClO2/c1-5-2(3)4/h1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [[Intramolecular alkylation of aromatic compounds. 35. Di- and tetrahydropyridinemethylindolines as potential precursors of ergolines] ]. | 2001 Jan |
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| Analysis of carnitine biosynthesis metabolites in urine by HPLC-electrospray tandem mass spectrometry. | 2002 Jun |
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| Large-scale synthesis of a persistent trityl radical for use in biomedical EPR applications and imaging. | 2007 Dec 15 |
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| Enantiomeric analysis of amino acids by using comprehensive two-dimensional gas chromatography. | 2007 Mar |
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| Characterization of the methoxy carbonyl radical formed via photolysis of methyl chloroformate at 193.3 nm. | 2007 Mar 15 |
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| The first solid enols of anhydrides. Structure, properties, and enol/anhydride equilibria(1). | 2007 Nov 23 |
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| New nordihydroguaiaretic acid derivatives as anti-HIV agents. | 2008 Mar 15 |
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| Corrrelation of the specific rates of solvolysis of ethyl fluoroformate using the extended Grunwald-Winstein equation. | 2009 Mar |
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| Use of empirical correlations to determine solvent effects in the solvolysis of S-methyl chlorothioformate. | 2010 May 25 |
Patents
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| Code System | Code | Type | Description | ||
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1116
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201-187-3
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6586
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RC6VA8OB2N
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METHYL CHLOROFORMATE
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DTXSID0024185
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79-22-1
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m7384
Created by
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C014667
Created by
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SUBSTANCE RECORD
