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620-17-7,MFCD00002311
Catalog No.:AA003JBX

620-17-7 | 3-Ethylphenol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
97%(GC)
in stock  
$24.00   $17.00
- +
25g
97%(GC)
in stock  
$72.00   $50.00
- +
100g
95%
in stock  
$261.00   $183.00
- +
500g
95%
in stock  
$1,092.00   $764.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003JBX
Chemical Name:
3-Ethylphenol
CAS Number:
620-17-7
Molecular Formula:
C8H10O
Molecular Weight:
122.1644
MDL Number:
MFCD00002311
SMILES:
CCc1cccc(c1)O
NSC Number:
8873
Properties
Properties
 
BP:
212°C at 760 mmHg  
Form:
Liquid  
MP:
-4 °C  
Refractive Index:
n20/D 1.533(lit.)  
Storage:
Inert atmosphere;Room Temperature;  

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:
2.4  

Literature

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

Journal: Chemical research in toxicology 20180521

Title: Development of enantioselective synthetic routes to (-)-kinamycin F and (-)-lomaiviticin aglycon.

Journal: Journal of the American Chemical Society 20121017

Title: Defensive secretions of the carabid beetle Chlaenius cordicollis: chemical components and their geographic patterns of variation.

Journal: Journal of chemical ecology 20120301

Title: The role of cow urine in the oviposition site preference of culicine and Anopheles mosquitoes.

Journal: Parasites & vectors 20110101

Title: Morpho-functional identification of abdominal olfactory receptors in the midge Culicoides imicola.

Journal: Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology 20101101

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

Journal: Biodegradation 20100401

Title: Differences in defensive volatiles of the forked fungus beetle, Bolitotherus cornutus, living on two species of fungus.

Journal: Journal of chemical ecology 20091101

Title: Modeling quality of premium spanish red wines from gas chromatography-olfactometry data.

Journal: Journal of agricultural and food chemistry 20090826

Title: A sex pheromone in the desert tenebrionid beetle Parastizopus armaticeps.

Journal: Journal of chemical ecology 20080801

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

Journal: Journal of molecular graphics & modelling 20061101

Title: Testing electrostatic complementarity in enzyme catalysis: hydrogen bonding in the ketosteroid isomerase oxyanion hole.

Journal: PLoS biology 20060401

Title: Susceptibility of newborn rats to 3-ethylphenol and 4-ethylphenol compared with that of young rats.

Journal: Congenital anomalies 20060301

Title: Structural basis of Src tyrosine kinase inhibition with a new class of potent and selective trisubstituted purine-based compounds.

Journal: Chemical biology & drug design 20060101

Title: Data processing and classification analysis of proteomic changes: a case study of oil pollution in the mussel, Mytilus edulis.

Journal: Proteome science 20060101

Title: Enrichment of cheeses manufactured from cow's and sheep's milk blends with sheep-like species-related alkylphenols.

Journal: Journal of agricultural and food chemistry 20050309

Title: Distribution of conjugates of alkylphenols in milk from different ruminant species.

Journal: Journal of dairy science 20050101

Title: Field studies on efficacy of host odour baits for the biting midge Culicoides impunctatus in Scotland.

Journal: Medical and veterinary entomology 20010601

Title: Genetic polymorphism in the human UGT1A6 (planar phenol) UDP-glucuronosyltransferase: pharmacological implications.

Journal: Pharmacogenetics 19971201

Title: 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.

Journal: Molecular pharmacology 19940101

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