2,2'-Dihydroxybenzophenone

Product Information

Molecular Formula:
C13H10O3
Molecular Weight:
214.22
Description
2,2'-Dihydroxybenzophenone (CAS# 835-11-0) is a useful research chemical.
Synonyms
bis(2-hydroxyphenyl)methanone
IUPAC Name
bis(2-hydroxyphenyl)methanone
Canonical SMILES
C1=CC=C(C(=C1)C(=O)C2=CC=CC=C2O)O
InChI
InChI=1S/C13H10O3/c14-11-7-3-1-5-9(11)13(16)10-6-2-4-8-12(10)15/h1-8,14-15H
InChI Key
YIYBRXKMQFDHSM-UHFFFAOYSA-N
Boiling Point
333 ℃ (estimate)
Melting Point
61-62.5 ℃ (lit.)
Purity
> 99.0 % (GC)
Density
1.1956 (rou gh estimate)
Appearance
Light yellow to yellow to orange powder to crystaline
Refractive Index
1.5090 (estimate)
LogP
2.32880

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
3.2
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
2
Exact Mass
214.062994177 g/mol
Monoisotopic Mass
214.062994177 g/mol
Topological Polar Surface Area
57.5Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
228
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-113817133-A Room-temperature self-crosslinking water-based nonionic polyurethane dispersion and preparation method and application thereof 2021-09-18
CN-112608516-A Multifunctional light-stable composition and preparation method thereof 2020-12-15
CN-111875791-A Preparation method of polyaryletherketone resin 2020-08-31
WO-2022043424-A1 Hydrolysis-resistant polycarbonate composition 2020-08-31
WO-2022029260-A1 Thermoplastic mixtures 2020-08-07
EP-3933059-A1 Process for the preparation of a polycarbonate 2020-06-29
WO-2021261195-A1 Optical film, optical film manufacturing method, transparent conductive film, and gas barrier film 2020-06-23
CN-111844328-A Anti-cracking method for wood 2020-06-22
JP-2022001623-A Resin composition and method for improving thermal conductivity 2020-06-22
EP-3922452-A1 Multilayer composite material 2020-06-08

Literatures

PMID Publication Date Title Journal
22091191 2011-08-01 (2-Hy-droxy-4-meth-oxy-phen-yl)(2-hy-droxy-phen-yl)methanone Acta crystallographica. Section E, Structure reports online
19640715 2009-09-01 A chemical screening approach reveals that indole fluorescence is quenched by pre-fibrillar but not fibrillar amyloid-beta Bioorganic & medicinal chemistry letters
16497524 2006-11-01 Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods Journal of molecular graphics & modelling
16132269 2005-10-01 Effects of helium-neon laser irradiation and local anesthetics on potassium channels in pond snail neurons Neuroscience and behavioral physiology
15694459 2005-02-15 Estrogenic and antiandrogenic activities of 17 benzophenone derivatives used as UV stabilizers and sunscreens Toxicology and applied pharmacology
11258977 2001-03-01 Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens Chemical research in toxicology
The molarity calculator equation

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

The dilution calculator equation

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

This equation is commonly abbreviated as: C1V1 = C2V2

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