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Sigma-Aldrich 185892 Ethyl chloroformate 97% CAS No.: 541-41-3 5 gr
Marka
Stok Kodu
LB.SA.185892-5G
Kısa Bilgi
Synonym(s): Chloroformic acid ethyl ester Linear Formula: ClCOOC2H5 CAS Number: 541-41-3 Molecular Weight: 108.52 UNSPSC Code: 12352100 NACRES: NA.22 PubChem Substance ID: 24851187 EC Number: 208-778-5 Beilstein/REAXYS Number: 385653 MDL number: MFCD00000644
| Sigma-Aldrich 185892 Ethyl chloroformate 97% CAS No.: 541-41-3 |
| Synonym(s): Chloroformic acid ethyl ester Linear Formula: ClCOOC2H5 CAS Number: 541-41-3 Molecular Weight: 108.52 UNSPSC Code: 12352100 NACRES: NA.22 PubChem Substance ID: 24851187 EC Number: 208-778-5 Beilstein/REAXYS Number: 385653 MDL number: MFCD00000644 |
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PROPERTIES
Product Name Ethyl chloroformate, 97%
InChI key RIFGWPKJUGCATF-UHFFFAOYSA-N InChI 1S/C3H5ClO2/c1-2-6-3(4)5/h2H2,1H3 SMILES string CCOC(Cl)=O vapor density 3.74 (vs air) vapor pressure 3.42 psi ( 20 °C) assay 97% form liquid autoignition temp. 842 °F refractive index n20/D 1.395 (lit.) bp 93 °C (lit.) mp −81 °C (lit.) solubility alcohol: miscible benzene: miscible chloroform: miscible diethyl ether: miscible water: insoluble density 1.135 g/mL at 25 °C (lit.) functional group chloro Quality Level 200 DESCRIPTION Application - Ethyl chloroformate was used in the synthesis of nitrile oxides[1]. - It was used as derivatization reagent to investigate stereochemical conversion of chiral non-steroidal anti-inflammatory drugs during derivatization reaction[2]. - It was used to develop flexible template strategy for the generation of nanometer-scale templates via dip-pen nanolithography[3]. - It was used as derivatization reagent in an enantiomeric analysis of amino acids by two-dimensional gas chromatography[4]. - It was also used with ammonia and cyanuric chloride to convert carboxylic acids to nitriles[5]. Packaging Derivatization reagent employed in an enantiomeric analysis of amino acids by two-dimensional gas chromatography.[4] Also used with ammonia and cyanuric chloride to convert carboxylic acids to nitriles.[5] |
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