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29692-57-7

29692-57-7 | Phenol, ethoxy-

CAS No: 29692-57-7 Catalog No: AG002Z4M MDL No:

Product Description

Catalog Number:
AG002Z4M
Chemical Name:
Phenol, ethoxy-
CAS Number:
29692-57-7
Molecular Formula:
C8H10O2
Molecular Weight:
138.1638
IUPAC Name:
2-ethoxyphenol
InChI:
InChI=1S/C8H10O2/c1-2-10-8-6-4-3-5-7(8)9/h3-6,9H,2H2,1H3
InChI Key:
MOEFFSWKSMRFRQ-UHFFFAOYSA-N
SMILES:
CCOc1ccccc1O
EC Number:
202-358-5
UNII:
878IW8P9PW
NSC Number:
1809

Properties

Complexity:
93.3  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
138.068g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
138.166g/mol
Monoisotopic Mass:
138.068g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
29.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.7  

Literature

Title Journal
2-Eth-oxy-6-{[1-(3-eth-oxy-2-hy-droxy-benz-yl)-1H-benzimidazol-2-yl]meth-yl}phenol nitro-methane monosolvate. Acta crystallographica. Section E, Structure reports online 20120601
2-Eth-oxy-6-[1-(3-eth-oxy-2-hy-droxy-benz-yl)-2,3-dihydro-1H-benzimidazol-2-yl]phenol acetonitrile monosolvate. Acta crystallographica. Section E, Structure reports online 20120501
(E)-N'-(3-Eth-oxy-4-hy-droxy-benzyl-idene)-4-meth-oxy-benzohydrazide. Acta crystallographica. Section E, Structure reports online 20120301
Synthesis, spectroscopy and antimicrobial activity of iron complexes of some smoke flavour compounds. Natural product research 20120101
Amalgamating metalloligands with coordination networks. Dalton transactions (Cambridge, England : 2003) 20100227
Differential detection of genetic Loci underlying stem and root lignin content in Populus. PloS one 20100101
(Z)-6-[(5-Chloro-2-hydroxy-phenyl)-aminomethyl-ene]-2-ethoxy-cyclo-hexa-2,4-dienone. Acta crystallographica. Section E, Structure reports online 20090901
A previously uncultured, paper mill Propionibacterium is able to degrade O-aryl alkyl ethers and various aromatic hydrocarbons. Chemosphere 20090601
Screening of dialkoxybenzenes and disubstituted cyclopentene derivatives against the cabbage looper, Trichoplusia ni, for the discovery of new feeding and oviposition deterrents. Journal of agricultural and food chemistry 20071212
Physiological, numerical and molecular characterization of alkyl ether-utilizing rhodococci. Environmental microbiology 20070601
Determination of vanillin and related flavor compounds in cocoa drink by capillary electrophoresis. Journal of chromatography. A 20070105
Formation and dissociation of intra-intermolecular hydrogen-bonded solute-solvent complexes: chemical exchange two-dimensional infrared vibrational echo spectroscopy. Journal of the American Chemical Society 20060308
Structure--activity relationships among novel phenoxybenzamine-related beta-chloroethylamines. Bioorganic & medicinal chemistry 20020501
Mechanism-based irreversible inactivation of horseradish peroxidase at 500 MPa. Biotechnology progress 20020101

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