2,2-Oxybisphenol

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Product Information

Molecular Formula:
C12H10O3
Molecular Weight:
202.21
Description
2,2-Oxybisphenol is an organic compound with anti-inflammatory and antioxidant properties. It is widely used in the study of cardiovascular abnormalities and neurodegenerative diseases.
Synonyms
Bis(2-hydroxyphenyl) Ether||||2-Hydroxyphenyl Ether||||2,2'-Oxybisphenol||||2,2'-Oxydiphenol
IUPAC Name
2-(2-hydroxyphenoxy)phenol
Canonical SMILES
C1=CC=C(C(=C1)O)OC2=CC=CC=C2O
InChI
InChI=1S/C12H10O3/c13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)14/h1-8,13-14H
InChI Key
VXHYVVAUHMGCEX-UHFFFAOYSA-N
Melting Point
123 °C
Purity
>98.0%(GC)
Appearance
White to Almost white powder to crystal

Safety Information

Hazards
H315:
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].

Computed Properties

XLogP3
2.7
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
175
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
WO-2022054897-A1 Curing agent composition for epoxy resins, epoxy resin composition, and coating material 2020-09-14
WO-2022043424-A1 Hydrolysis-resistant polycarbonate composition 2020-08-31
WO-2022034898-A1 Thermoplastic resin composition for optical material, molded article, compounding agent, method for producing thermoplastic resin composition, and method for improving transmissivity 2020-08-13
WO-2022029260-A1 Thermoplastic mixtures 2020-08-07
CN-112010787-A Agricultural preparation dispersant, preparation method and application thereof 2020-07-29
JP-2022021149-A A composition, a synthetic resin composition containing the composition, and a molded product thereof. 2020-07-21
WO-2022014338-A1 Stabilizer composition, vinyl chloride resin composition containing same, and molded body of same 2020-07-17
JP-2022014019-A Polycarbonate resin composition 2020-07-06
JP-2022013866-A Temperature control indicator and how to use it 2020-06-30
EP-3933059-A1 Process for the preparation of a polycarbonate 2020-06-29

Literatures

PMID Publication Date Title Journal
16539372 2006-03-23 Enantiomer discrimination illustrated by the high resolution crystal structures of type 4 phosphodiesterase Journal of medicinal chemistry
15491144 2004-10-26 Role of inhibitor aliphatic chain in the thermodynamics of inhibitor binding to Escherichia coli enoyl-ACP reductase and the Phe203Leu mutant: a proposed mechanism for drug resistance Biochemistry
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
3821 1975-09-01 [Automatic method for determination of serum antistreptolysin] Quaderni Sclavo di diagnostica clinica e di laboratorio
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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