HYDROBENZOIN

Product Information

Molecular Formula:
C14H14O2
Molecular Weight:
214.25976
Description
Hydrobenzoin is an ethanediol.
Synonyms
1,2-diphenylethane-1,2-diol; MESO-1,2-DIPHENYL-1,2-ETHANEDIOL 96+%; 1,2-Ethanediol, 1,2-diphenyl-; HYDROBENZOIN / 1,2-DIPHENYL-1,2-ETHANEDIOL; 1,2-Bisphenyl-1,2-ethanediol; 1,2-Diphenylethylene glycol
IUPAC Name
1,2-diphenylethane-1,2-diol
Canonical SMILES
C1=CC=C(C=C1)C(C(C2=CC=CC=C2)O)O
InChI
InChI=1S/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H
InChI Key
IHPDTPWNFBQHEB-UHFFFAOYSA-N
Flash Point
Not applicable

Computed Properties

XLogP3
1.6
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
3
Exact Mass
214.099379685 g/mol
Monoisotopic Mass
214.099379685 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
171
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
2
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-114088803-A Analytical reagent and method for separating phenyl-substituted ethylene glycol enantiomer 2021-10-20
CN-113980259-A Method for preparing polycarbonate by using 1,1,3,3,4,4,6, 6-octamethyltetrahydropentene-2, 5-diol 2021-10-14
CN-113842908-A Regulation and control of C-C bond aerobic oxidative cracking product by vanadium oxide-based photocatalyst 2021-09-27
CN-113671068-A Method for analyzing environmental pollutant targeting exposure component in blood plasma and application thereof 2021-07-27
CN-113476602-A Preparation of novel high photothermal conversion efficiency cyanine photosensitizer and self-targeting phototherapy of tumor 2021-07-02
CN-113512888-A Washing fabric structure based on thermosensitive color development technology 2021-06-18
CN-113087667-A Synthesis method of imidazolidinone derivative 2021-03-24
CN-113070096-A Biomass oxidative cracking catalyst based on modified H-Beta molecular sieve, and preparation method and application thereof 2021-03-22
CN-112961098-A Organic fluorescent material containing pyrene unit and having aggregation induced luminescence, and preparation method and application thereof 2021-02-09
CN-112592465-A Osmium-containing heteropentadiyne conjugated polymer with main chain and preparation method and application thereof 2020-11-06

Literatures

PMID Publication Date Title Journal
22322664 2012-03-28 Mechanism and optimisation of the homoboroproline bifunctional catalytic asymmetric aldol reaction: Lewis acid tuning through in situ esterification Organic & biomolecular chemistry
22380404 2012-03-01 Effects of Litchi chinensis fruit isolates on prostaglandin E(2) and nitric oxide production in J774 murine macrophage cells BMC complementary and alternative medicine
21871626 2011-10-07 Methods for determination of all binding parameters in systems with simultaneous borate and cyclodextrin complexation Journal of chromatography. A
21899850 2011-10-07 Morphological modification of nanostructured ultrathin-layer chromatography stationary phases Journal of chromatography. A
21761523 2011-08-22 Asymmetric autocatalysis: triggered by chiral isotopomer arising from oxygen isotope substitution Angewandte Chemie (International ed. in English)
21837163 2011-07-01 2,4,5-Triphenyl-1,3,2-dioxa-phospho-lan-2-one Acta crystallographica. Section E, Structure reports online
21161974 2011-06-06 SERS chiral recognition and quantification of enantiomers through cyclodextrin supramolecular complexation Chemphyschem : a European journal of chemical physics and physical chemistry
21706497 2011-06-01 Chiral selectivity of guanosine media in capillary electrophoresis Electrophoresis
21500208 2011-05-01 Chiral micellar electrokinetic chromatography-atmospheric pressure photoionization of benzoin derivatives using mixed molecular micelles Electrophoresis
22043241 2011-01-01 Directed ortho,ortho'-dimetalation of hydrobenzoin: Rapid access to hydrobenzoin derivatives useful for asymmetric synthesis Beilstein journal of organic chemistry
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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