Diethyl Methylphosphonate - CAS 683-08-9
Catalog: |
BB033519 |
Product Name: |
Diethyl Methylphosphonate |
CAS: |
683-08-9 |
Synonyms: |
1-[ethoxy(methyl)phosphoryl]oxyethane; 1-[ethoxy(methyl)phosphoryl]oxyethane |
IUPAC Name: | 1-[ethoxy(methyl)phosphoryl]oxyethane |
Description: | Diethyl Methylphosphonate (CAS# 683-08-9) is a useful research chemical. |
Molecular Weight: | 152.13 |
Molecular Formula: | C5H13O3P |
Canonical SMILES: | CCOP(=O)(C)OCC |
InChI: | InChI=1S/C5H13O3P/c1-4-7-9(3,6)8-5-2/h4-5H2,1-3H3 |
InChI Key: | NYYLZXREFNYPKB-UHFFFAOYSA-N |
Boiling Point: | 194 °C |
Density: | 1.041 g/cm3 |
MDL: | MFCD00009813 |
LogP: | 1.88230 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-207793121-U | A kind of device of synthesizing methyl diethyl phosphite | 20180115 |
CN-108727427-A | A kind of succinct glufosinate-ammonium synthetic method | 20170424 |
CN-107236002-A | A kind of synthetic method of methylisothiouronium methylphosphite diethylester | 20160406 |
CN-104725416-B | Glufosinate-ammonium intermediate methylisothiouronium methylphosphite diethylester continuous separation method and device | 20150325 |
WO-2015196118-A1 | Alternative nucleic acid molecules and uses thereof | 20140619 |
PMID | Publication Date | Title | Journal |
22673812 | 20120720 | Zirconia coated stir bar sorptive extraction combined with large volume sample stacking capillary electrophoresis-indirect ultraviolet detection for the determination of chemical warfare agent degradation products in water samples | Journal of chromatography. A |
22018853 | 20120410 | Dust as a collection media for contaminant source attribution | Forensic science international |
22326187 | 20120316 | Determination of S-2-(N,N-diisopropylaminoethyl)- and S-2-(N,N-diethylaminoethyl) methylphosphonothiolate, nerve agent markers, in water samples using strong anion-exchange disk extraction, in vial trimethylsilylation, and gas chromatography-mass spectrometry analysis | Journal of chromatography. A |
21905719 | 20111021 | Catalytic degradation of the nerve agent VX by water-swelled polystyrene-supported ammonium fluorides | The Journal of organic chemistry |
20509631 | 20100705 | Activation of a PARACEST agent for MRI through selective outersphere interactions with phosphate diesters | Inorganic chemistry |
Complexity: | 103 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 152.06023127 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 152.06023127 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 35.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.4 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Phosphorus Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS