Benzopinacol - CAS 464-72-2
Catalog: |
BB026138 |
Product Name: |
Benzopinacol |
CAS: |
464-72-2 |
Synonyms: |
1,1,2,2-tetraphenylethane-1,2-diol |
IUPAC Name: | 1,1,2,2-tetraphenylethane-1,2-diol |
Description: | 1,1,2,2-Tetraphenyl-1,2-ethanediol (CAS# 464-72-2) is a useful research chemical. |
Molecular Weight: | 366.45 |
Molecular Formula: | C26H22O2 |
Canonical SMILES: | C1=CC=C(C=C1)C(C2=CC=CC=C2)(C(C3=CC=CC=C3)(C4=CC=CC=C4)O)O |
InChI: | InChI=1S/C26H22O2/c27-25(21-13-5-1-6-14-21,22-15-7-2-8-16-22)26(28,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20,27-28H |
InChI Key: | MFEWNFVBWPABCX-UHFFFAOYSA-N |
Boiling Point: | 506.9 °C at 760 mmHg |
Melting Point: | 184-186 °C |
Purity: | 95 % |
Density: | 1.198 g/cm3 |
Appearance: | White crystalline powder |
Storage: | Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. |
LogP: | 4.85860 |
Publication Number | Title | Priority Date |
CN-113501917-A | Environment-friendly impregnating resin with high thermal conductivity coefficient and preparation method and application thereof | 20210730 |
CN-113045865-A | Photocuring method of large-area dark fiber cloth epoxy composite material | 20210518 |
CN-111607186-A | Preparation method of low-protein adsorption antifouling waterproof plastic particles | 20200624 |
CN-111606793-A | Method for preparing substituted carbonyl compound by using molecular sieve to catalyze pinacol rearrangement reaction | 20200610 |
US-2021309567-A1 | Self-healing optical fibers and the compositions used to create the same | 20200403 |
PMID | Publication Date | Title | Journal |
20177746 | 20100501 | Synthesis, spectroscopy and photochemistry of novel branched fluorescent nitro-stilbene derivatives with benzopheonone groups | Journal of fluorescence |
16715413 | 20060701 | Synthesis of alpha-trifluoromethyl alpha-amino acids with aromatic, heteroaromatic and ferrocenyl subunits in the side chain | Amino acids |
16674072 | 20060512 | BF3.2CF3CH2OH (BF3.2TFE), an efficient superacidic catalyst for some organic synthetic transformations | The Journal of organic chemistry |
16146386 | 20050915 | Reduction of benzophenone by SmI2: the role of proton donors in determining product distribution | Organic letters |
11686699 | 20011107 | Synthesis, structure, and reactions of (acylimino)triaryl-lambda(5)-bismuthanes: first comparative study of the (acylimino)pnictorane series | Journal of the American Chemical Society |
Complexity: | 383 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 366.16197994 |
Formal Charge: | 0 |
Heavy Atom Count: | 28 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 366.16197994 |
Rotatable Bond Count: | 5 |
Topological Polar Surface Area: | 40.5 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 4.9 |
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