Allyl bisphenol A
Product Information
Molecular Formula
C21H24O2
Molecular Weight
308.41406
Description
Allyl bisphenol A is a widely employed chemical compound in the biomedical sector and showcases remarkable pharmacological attributes encompassing potent antibacterial and anti-inflammatory properties. Its predominant application revolves around the creation of pharmaceutical agents directed against bacterial infections and inflammatory ailments. The immense research elucidating its therapeutic capacity endows this compound with indispensable significance in the realm of biomedical exploration and pharmaceutical innovation.
Synonyms
AllylbisphenolA; 2,2'-DiallylbisphenolA; 1745-89-7; DiallylbisphenolA; 4,4'-(Propane-2,2-diyl)bis(2-allylphenol); SBB057159
IUPAC Name
4-[2-(4-hydroxy-3-prop-2-enylphenyl)propan-2-yl]-2-prop-2-enylphenol
SMILES
CC(C)(C1=CC(=C(C=C1)O)CC=C)C2=CC(=C(C=C2)O)CC=C
InChI
InChI=1S/C21H24O2/c1-5-7-15-13-17(9-11-19(15)22)21(3,4)18-10-12-20(23)16(14-18)8-6-2/h5-6,9-14,22-23H,1-2,7-8H2,3-4H3
InChI Key
WOCGGVRGNIEDSZ-UHFFFAOYSA-N
Boiling Point
445.2°C at 760 mmHg
Melting Point
-52°C
Flash Point
235.4 °CF - closed cup
Purity
95%
Density
1.08
Appearance
Light yellow or brown liquid
Storage
Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition sources and untrained individuals. Secure and label area. Protect containers/cylinders from physical damage.
Refractive Index
n20/D 1.587 (lit.)
Safety Information
Hazards
H314 - H317
Precautionary Statement
P280 - P305 + P351 + P338 - P310
Computed Properties
XLogP3
6.1
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
6
Exact Mass
308.177630004 g/mol
Monoisotopic Mass
308.177630004 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
23
Formal Charge
0
Complexity
365
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-114015046-A | Modified bismaleimide prepolymer, composition prepared from modified bismaleimide prepolymer, prepreg and laminated board of prepreg | 2021-12-07 |
| JP-2022020781-A | Curable resin composition and laminate | 2021-11-11 |
| CN-113845775-A | Preparation method of hyperbranched polymer modified boron nitride heat-conducting and insulating composite material | 2021-11-08 |
| CN-114147991-A | Connecting ring forming and bonding method | 2021-11-08 |
| CN-113980582-A | Light, heat and moisture curable adhesive and preparation method thereof | 2021-10-08 |
| CN-113861603-A | Halogen-free resin composition for high-frequency high-speed copper-clad plate and preparation method and application thereof | 2021-09-27 |
| CN-113563542-A | Polyacrylamide copolymer, polymer profile control agent and preparation method thereof | 2021-09-24 |
| CN-113563542-B | Polyacrylamide copolymer, polymer profile control agent and preparation method thereof | 2021-09-24 |
| CN-113736120-A | Preparation method of N-spiro quaternary ammonium salt functionalized polyaryletherketone anion exchange membrane for fuel cell | 2021-09-08 |
| CN-113736401-A | High-heat-resistance single-component adhesive and preparation method thereof | 2021-09-06 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 17587572 | 2007-08-15 | Synthesis, cytotoxicity, and antiviral activities of new neolignans related to honokiol and magnolol | Bioorganic & medicinal chemistry letters |
