90-00-6 | 2-Ethylphenol

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$17.00	$12.00
25g	95%	in stock	$31.00	$22.00
100g	96%	in stock	$90.00	$63.00
500g	96%	in stock	$251.00	$176.00

Description

• Catalog Number: AI60267
• Chemical Name: 2-Ethylphenol
• CAS Number: 90-00-6
• Molecular Formula: C8H10O
• Molecular Weight: 122.1644
• MDL Number: MFCD00002249
• SMILES: CCC1=CC=CC=C1O
• NSC Number: 10112

Computed Properties

• Complexity: 80.6
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.5

Literature

• Activation of TRPV3 by Wood Smoke Particles and Roles in Pneumotoxicity.

  Chemical research in toxicology 20180521

• Antifungal efficacy of some natural phenolic compounds against significant pathogenic and toxinogenic filamentous fungi.

  Chemosphere 20131001

• Enzymatic synthesis of rose aromatic ester (2-phenylethyl acetate) by lipase.

  Journal of the science of food and agriculture 20120815

• Chemical activation of bituminous coal for hampering oligomerization of organic contaminants.

  Journal of hazardous materials 20111215

• Insecticidal properties of phenols on Culex quinquefasciatus Say and Musca domestica L.

  Parasitology research 20111201

• Preparation of metal wire supported solid-phase microextraction fiber coated with multi-walled carbon nanotubes.

  Journal of separation science 20110901

• Quantitative analysis of euglobals in Eucalyptus loxophleba leaves by qNMR.

  Natural product communications 20110901

• Comparison of volatile components in Chinese traditional pickled peppers using HS-SPME-GC-MS, GC-O and multivariate analysis.

  Natural product research 20101201

• Enantioselective synthesis of (R)-bufuralol via dynamic kinetic resolution in the key step.

  The Journal of organic chemistry 20100702

• Isolation and characterization of a novel 2-sec-butylphenol-degrading bacterium Pseudomonas sp. strain MS-1.

  Biodegradation 20100401

• 9-(2-Ethyl-phenoxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate.

  Acta crystallographica. Section E, Structure reports online 20100401

• Experimental and computational studies on the iridium activation of aliphatic and aromatic C-H bonds of alkyl aryl ethers and related molecules.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090914

• Parallel synthesis of O-phenoxyethyl and O-adamantyl N-acyl thiocarbamates endowed with antiproliferative activity.

  Archiv der Pharmazie 20090601

• Mechanism of ethylbenzene-induced mouse-specific lung tumor: metabolism of ethylbenzene by rat, mouse, and human liver and lung microsomes.

  Toxicological sciences : an official journal of the Society of Toxicology 20090201

• The effect of functional groups on oligomerization of phenolics on activated carbon.

  Journal of hazardous materials 20070905

• Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.

  Journal of molecular graphics & modelling 20061101

• Metabolic activation of carcinogenic ethylbenzene leads to oxidative DNA damage.

  Chemico-biological interactions 20041207

• Adsorption of phenolics on activated carbon--impact of pore size and molecular oxygen.

  Chemosphere 20040501

• Inhibition of the acetoclastic methanogenic activity by phenol and alkyl phenols.

  Environmental technology 20030801

• Toxicity and kinetic parameters of the aerobic biodegradation of the phenol and alkylphenols by a mixed culture.

  Biotechnology letters 20030401

• Schiff bis bases: analytical reagents. II. Spectrophotometric determination of manganese from pharmaceutical forms.

  Journal of pharmaceutical and biomedical analysis 20020201

• Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens.

  Chemical research in toxicology 20010301

• Determination of phenols in soil by supercritical fluid extraction-capillary electrochromatography.

  Journal of chromatography. A 20010112

• A recombinant phenobarbital-inducible rat liver UDP-glucuronosyltransferase (UDP-glucuronosyltransferase 2B1) stably expressed in V79 cells catalyzes the glucuronidation of morphine, phenols, and carboxylic acids.

  Molecular pharmacology 19940101