1,3-Dibenzoylpropane - CAS 6263-83-8
Catalog: |
BB031705 |
Product Name: |
1,3-Dibenzoylpropane |
CAS: |
6263-83-8 |
Synonyms: |
1,5-diphenylpentane-1,5-dione |
IUPAC Name: | 1,5-diphenylpentane-1,5-dione |
Description: | 1,3-Dibenzoylpropane (CAS# 6263-83-8) is a useful research chemical compound. |
Molecular Weight: | 252.31 |
Molecular Formula: | C17H16O2 |
Canonical SMILES: | C1=CC=C(C=C1)C(=O)CCCC(=O)C2=CC=CC=C2 |
InChI: | InChI=1S/C17H16O2/c18-16(14-8-3-1-4-9-14)12-7-13-17(19)15-10-5-2-6-11-15/h1-6,8-11H,7,12-13H2 |
InChI Key: | YOLLTWVIOASMFW-UHFFFAOYSA-N |
Boiling Point: | 421.7 °C at 760 mmHg |
Density: | 1.097 g/cm3 |
Appearance: | White to beige solid, powder or crystals |
MDL: | MFCD00051401 |
LogP: | 3.92250 |
Publication Number | Title | Priority Date |
JP-2020196771-A | Method for forming composition, resist underlayer film, resist underlayer film, and method for producing patterned substrate | 20190530 |
WO-2019142208-A1 | Ambient temperature curable non-isocyanate polyhydroxyalkylurethane moieties with aldehyde cross linker | 20180116 |
RU-2657250-C1 | Method for preparation of 2-acyl(aroyl)-7-imino-6-oxabicyclo[3.2.1]octane-1,8,8-tricarbonitriles | 20171113 |
US-2018271803-A1 | Compositions and methods for treatment or prevention of oral mucositis | 20150902 |
US-2020206156-A1 | Compositions and Methods for Treatment or Prevention of Oral Mucositis | 20150902 |
PMID | Publication Date | Title | Journal |
21924245 | 20111215 | Suppression of pro-inflammatory and proliferative pathways by diferuloylmethane (curcumin) and its analogues dibenzoylmethane, dibenzoylpropane, and dibenzylideneacetone: role of Michael acceptors and Michael donors | Biochemical pharmacology |
19886613 | 20091203 | Optical and electron paramagnetic resonance studies of the excited states of 4-tert-butyl-4'-methoxydibenzoylmethane and 4-tert-butyl-4'-methoxydibenzoylpropane | The journal of physical chemistry. A |
21200748 | 20071206 | 1,5,6-Triphenyl-8-oxa-7-selena-6-phos-phabicyclo-[3.2.1]octane-6-selone | Acta crystallographica. Section E, Structure reports online |
12812469 | 20030625 | Is it possible to estimate the enantioselectivity of a chiral catalyst from its racemic mixture? | Journal of the American Chemical Society |
Complexity: | 266 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 252.115029749 |
Formal Charge: | 0 |
Heavy Atom Count: | 19 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 252.115029749 |
Rotatable Bond Count: | 6 |
Topological Polar Surface Area: | 34.1 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.2 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS