200,000+ products from a single source!

sales@angenechem.com

Home > Other Building Blocks > 2174-64-3

2174-64-3

2174-64-3 | 3-Hydroxy-5-methoxyphenol

CAS No: 2174-64-3 Catalog No: AG0033JE MDL No:MFCD00002285

Product Description

Catalog Number:
AG0033JE
Chemical Name:
3-Hydroxy-5-methoxyphenol
CAS Number:
2174-64-3
Molecular Formula:
C7H8O3
Molecular Weight:
140.1366
MDL Number:
MFCD00002285
IUPAC Name:
5-methoxybenzene-1,3-diol
InChI:
InChI=1S/C7H8O3/c1-10-7-3-5(8)2-6(9)4-7/h2-4,8-9H,1H3
InChI Key:
HDVRLUFGYQYLFJ-UHFFFAOYSA-N
SMILES:
COc1cc(O)cc(c1)O
EC Number:
218-532-9
UNII:
6201E0JIF3

Properties

Complexity:
95  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
140.047g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
140.138g/mol
Monoisotopic Mass:
140.047g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
49.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.3  

Literature

Title Journal
(2,4-Dihy-droxy-6-meth-oxy-phen-yl)(3,5-dihy-droxy-phen-yl)methanone monohydrate. Acta crystallographica. Section E, Structure reports online 20111001
1-(2,6-Dihydr-oxy-4-methoxy-phen-yl)-3-phenyl-propan-1-one. Acta crystallographica. Section E, Structure reports online 20100501
Stopped-flow kinetic study of the aroxyl radical-scavenging action of catechins and vitamin C in ethanol and micellar solutions. Journal of agricultural and food chemistry 20080625
Kinetic study of the quenching reaction of singlet oxygen by tea catechins in ethanol solution. Free radical biology & medicine 20050915
Structure-activity relationship of the tocopherol-regeneration reaction by catechins. Free radical biology & medicine 20050501
The key role of phloroglucinol O-methyltransferase in the biosynthesis of Rosa chinensis volatile 1,3,5-trimethoxybenzene. Plant physiology 20040501
Two O-methyltransferases isolated from flower petals of Rosa chinensis var. spontanea involved in scent biosynthesis. Journal of bioscience and bioengineering 20030101

© 2019 Angene International Limited. All rights Reserved.