4-Benzoylbiphenyl - CAS 2128-93-0
Catalog: |
BB016754 |
Product Name: |
4-Benzoylbiphenyl |
CAS: |
2128-93-0 |
Synonyms: |
phenyl-(4-phenylphenyl)methanone; phenyl-(4-phenylphenyl)methanone |
IUPAC Name: | phenyl-(4-phenylphenyl)methanone |
Description: | 4-Benzoylbiphenyl (CAS# 2128-93-0) is a reagent used in the synthesis of multicolored mechanochromic luminogen molecules. |
Molecular Weight: | 258.31 |
Molecular Formula: | C19H14O |
Canonical SMILES: | C1=CC=C(C=C1)C2=CC=C(C=C2)C(=O)C3=CC=CC=C3 |
InChI: | InChI=1S/C19H14O/c20-19(17-9-5-2-6-10-17)18-13-11-16(12-14-18)15-7-3-1-4-8-15/h1-14H |
InChI Key: | LYXOWKPVTCPORE-UHFFFAOYSA-N |
Boiling Point: | 245 °C / 9 mmHg |
Melting Point: | 102 °C |
Flash Point: | 280.4 °F |
Purity: | 99 % |
Density: | 1.266 g/cm3 |
Appearance: | White to orange to green powder to crystal |
MDL: | MFCD00003079 |
LogP: | 4.58460 |
Publication Number | Title | Priority Date |
CN-113462346-A | UV/moisture dual-curing polyurethane hot melt adhesive with high initial adhesion and excellent drop resistance, and preparation method and application thereof | 20210727 |
CN-113416477-A | Photosensitive phytic acid doped polyaniline-based ultraviolet-curing anticorrosive paint and preparation method thereof | 20210702 |
CN-113429724-A | Hydrogel of lubricating coating, preparation method of hydrogel, hydrogel freeze-dried powder and application | 20210622 |
CN-113249039-A | Optical adhesive | 20210616 |
CN-113372491-A | Low-shrinkage high-bonding-strength boiling-resistant resin, adhesive and preparation method thereof | 20210615 |
PMID | Publication Date | Title | Journal |
21107368 | 20101201 | An efficient organocatalytic method for constructing biaryls through aromatic C-H activation | Nature chemistry |
20734309 | 20101004 | Structural basis for the improved potency of peroxisome proliferator-activated receptor (PPAR) agonists | ChemMedChem |
21580736 | 20100327 | (Biphenyl-4-yl)(phen-yl)methanone | Acta crystallographica. Section E, Structure reports online |
16970360 | 20060921 | Effects of localized triplet exciton on reactivity of photoinduced omega-bond dissociation in naphthyl phenyl ketones having pi,pi* lowest triplet (T1) states studied by laser flash photolysis | The journal of physical chemistry. A |
16311988 | 20060208 | Properties of excited ketyl radicals of benzophenone analogues affected by the size and electronic character of the aromatic ring systems | Chemistry (Weinheim an der Bergstrasse, Germany) |
Complexity: | 302 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 258.104465066 |
Formal Charge: | 0 |
Heavy Atom Count: | 20 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 258.104465066 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 17.1 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 4.9 |
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