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1195-09-1

1195-09-1 | Phenol, 2-methoxy-5-methyl-

CAS No: 1195-09-1 Catalog No: AG000P7U MDL No:MFCD00040901

Product Description

Catalog Number:
AG000P7U
Chemical Name:
Phenol, 2-methoxy-5-methyl-
CAS Number:
1195-09-1
Molecular Formula:
C8H10O2
Molecular Weight:
138.1638
MDL Number:
MFCD00040901
IUPAC Name:
2-methoxy-5-methylphenol
InChI:
InChI=1S/C8H10O2/c1-6-3-4-8(10-2)7(9)5-6/h3-5,9H,1-2H3
InChI Key:
IFNDEOYXGHGERA-UHFFFAOYSA-N
SMILES:
COc1ccc(cc1O)C
EC Number:
214-791-7
UNII:
AV5V76OU33

Properties

Complexity:
103  
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:
1  
Topological Polar Surface Area:
29.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.1  

Literature

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Defensive secretions of the carabid beetle Chlaenius cordicollis: chemical components and their geographic patterns of variation. Journal of chemical ecology 20120301
Studies of a ring-cleaving dioxygenase illuminate the role of cholesterol metabolism in the pathogenesis of Mycobacterium tuberculosis. PLoS pathogens 20090301
Effect of grain type and toasting conditions of barrels on the concentration of the volatile substances released by the wood and on the sensory characteristics of Montepulciano d'Abruzzo. Journal of food science 20080901
Structural analogues of homoeriodictyol as flavor modifiers. Part III: short chain gingerdione derivatives. Journal of agricultural and food chemistry 20080813
The binding site for neohesperidin dihydrochalcone at the human sweet taste receptor. BMC structural biology 20070101
(Z)-2-(3-hydroxy-4-methoxybenzylidene)-1-azabicyclo[2.2.2]octan-3-one. Acta crystallographica. Section C, Crystal structure communications 20031101
Novel benzylidene-9(10H)-anthracenones as highly active antimicrotubule agents. Synthesis, antiproliferative activity, and inhibition of tubulin polymerization. Journal of medicinal chemistry 20030717

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