4,4'-Oxydiphenol
Product Information
Molecular Formula
C12H10O3
Molecular Weight
202.21
Description
4,4'-Dihydroxydiphenyl ether is a natural product found in Allium tuberosum.
Synonyms
BIS(4-HYDROXYPHENYL) ETHER; 4',4-OXIDIPHENOL; 4',4-OXYDIPHENOL; 4,4'-OXYDIPHENOL; 4',4-DIHYDROXYDIPHENYL ETHER; 4,4'-DIHYDROXYDIPHENYL ETHER
IUPAC Name
4-(4-hydroxyphenoxy)phenol
SMILES
C1=CC(=CC=C1O)OC2=CC=C(C=C2)O
InChI
InChI=1S/C12H10O3/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12/h1-8,13-14H
InChI Key
NZGQHKSLKRFZFL-UHFFFAOYSA-N
Boiling Point
300.32°C (rough estimate)
Melting Point
163-168 °C
Purity
>98.0%(GC)
Density
1.288 g/cm3
Appearance
off-white amorphous powder
Refractive Index
1.5430 (estimate)
Safety Information
Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].
Computed Properties
XLogP3
2
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
2
Exact Mass
202.062994177 g/mol
Monoisotopic Mass
202.062994177 g/mol
Topological Polar Surface Area
49.7Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
159
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-114181053-A | Preparation method of diphenol monomer with lateral group containing trifluoromethyl and polyarylether polymer thereof | 2021-12-29 |
| CN-114085165-A | alpha-H-containing cyano modified acrylate resin and preparation method and application thereof | 2021-11-25 |
| CN-113896619-A | Preparation method of 4,4' -dibromodiphenyl ether | 2021-11-01 |
| CN-113637153-A | Multi-block polyether type high-molecular surfactant and preparation method and application thereof | 2021-10-18 |
| CN-113637154-A | Nonionic polyether type high-molecular surfactant and preparation method and application thereof | 2021-10-18 |
| CN-113637155-A | Anionic polyether type high-molecular surfactant and preparation method thereof | 2021-10-18 |
| CN-113996272-A | Molecularly imprinted polymer and preparation method and application thereof | 2021-10-13 |
| CN-113788803-A | Glycidyl ether type four-functionality epoxy resin, cured product thereof and preparation method thereof | 2021-09-13 |
| CN-113754861-A | Polycyclic aryl hyperbranched epoxy resin, preparation method thereof, photoluminescent solution and anticorrosive paint obtained by polycyclic aryl hyperbranched epoxy resin and application of photoluminescent solution and anticorrosive paint | 2021-09-09 |
| CN-113603970-A | Synergistic flame-retardant polypropylene composite material and preparation method thereof | 2021-08-26 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 19794917 | 2009-09-01 | Bioimaging probes for reactive oxygen species and reactive nitrogen species | Journal of clinical biochemistry and nutrition |
| 14736233 | 2004-01-29 | Inhibition of the bacterial enoyl reductase FabI by triclosan: a structure-reactivity analysis of FabI inhibition by triclosan analogues | Journal of medicinal chemistry |
| 1038 | 1975-12-15 | Beef liver L-Glutamate dehydrogenase mechanism: presteady state study of the catalytic reduction of 2.oxoglutarate by NADPH | Biochemical and biophysical research communications |
