Methyl phenoxyacetate - CAS 2065-23-8
Catalog: |
BB016129 |
Product Name: |
Methyl phenoxyacetate |
CAS: |
2065-23-8 |
Synonyms: |
methyl 2-phenoxyacetate |
IUPAC Name: | methyl 2-phenoxyacetate |
Description: | Methyl phenoxyacetate (CAS# 2065-23-8) is a chemical reagent for the transesterification reactions. Also, used in the synthesis of a β-lactam intermediate used in the synthesis of Loracarbef (L469550), an antibiotic, a synthetic carbacephem analogue of cefaclor, and is more stable chemically. |
Molecular Weight: | 166.17 |
Molecular Formula: | C9H10O3 |
Canonical SMILES: | COC(=O)COC1=CC=CC=C1 |
InChI: | InChI=1S/C9H10O3/c1-11-9(10)7-12-8-5-3-2-4-6-8/h2-6H,7H2,1H3 |
InChI Key: | BZCKRPHEZOHHBK-UHFFFAOYSA-N |
Boiling Point: | 243 °C |
Purity: | 98 % |
Density: | 1.149 g/cm3 |
Appearance: | Colorless to yellow liquid |
MDL: | MFCD00010227 |
LogP: | 1.23840 |
GHS Hazard Statement: | H315 (98.92%): 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 |
RU-2020132735-A | PHARMACEUTICAL COMPOSITION OF OXYETHYLAMMONIUM METHYLPHENOXYACETATE | 20201005 |
RU-2744757-C1 | A means of increasing the level of lactoferrin in the body | 20200727 |
RU-2749347-C1 | Preparation modulating ferritin concentration in blood serum | 20200313 |
CN-110357729-A | A kind of photosynthetic biological agent of enhancing pomegranate | 20190823 |
RU-2701178-C1 | Method of accelerating corneal healing accompanying mechanical injuries | 20190710 |
PMID | Publication Date | Title | Journal |
15633752 | 20041217 | Dicarboxylic degradation products of nonylphenol polyethoxylates: synthesis and identification by gas chromatography-mass spectrometry using electron and chemical ionization modes | Journal of chromatography. A |
14760696 | 20040305 | Combinatorial formulation of biocatalyst preparations for increased activity in organic solvents: salt activation of penicillin amidase | Biotechnology and bioengineering |
12816466 | 20030627 | Synthesis of functionalized porphyrins as oxygen ligand receptors | The Journal of organic chemistry |
Complexity: | 139 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 166.062994177 |
Formal Charge: | 0 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 166.062994177 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 35.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.4 |
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