Benzene,2-ethenyl-1,4-dimethyl-
Product Information
Molecular Formula
C10H12
Molecular Weight
132.2
Description
Benzene,2-ethenyl-1,4-dimethyl is a chemical compound with extensive applications in the biomedical industry and is utilized in the drug development of various diseases. Its potential applications include the treatment of cancer, as it exhibits anticancer properties. Additionally, it is used as an intermediate in the synthesis of pharmaceutical drugs targeting different ailments.
Synonyms
2,5-DIMETHYLSTYRENE; 1,4-Dimethyl-2-ethenylbenzene; 1,4-Dimethyl-2-vinylbenzene; 1-ethenyl-2,5-dimethylbenzene; 2,5-dimethyl-styren; 2-ethenyl-1,4-dimethylbenzene; benzene,1-ethenyl-2,5-dimethyl-; Styrene, 2,5-dimethyl-
IUPAC Name
2-ethenyl-1,4-dimethylbenzene
SMILES
CC1=CC(=C(C=C1)C)C=C
InChI
InChI=1S/C10H12/c1-4-10-7-8(2)5-6-9(10)3/h4-7H,1H2,2-3H3
InChI Key
DBWWINQJTZYDFK-UHFFFAOYSA-N
Boiling Point
71-72 °C/10 mmHg (lit.)
Melting Point
−35 °C (lit.)
Flash Point
147.2 °CF - closed cup
Purity
0.98
Density
0.893g/cm3
Storage
2-8°C
Refractive Index
n20/D 1.539 (lit.)
Safety Information
Hazards
H315 - H319 - H335
Precautionary Statement
P302 + P352 - P305 + P351 + P338
Computed Properties
XLogP3
3.4
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
1
Exact Mass
132.093900383 g/mol
Monoisotopic Mass
132.093900383 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
115
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-113880873-A | Hydroboration reaction method for catalyzing olefin by calcium halide | 2021-10-25 |
| CN-113698338-A | Preparation method of styrene double oxidation product | 2021-09-29 |
| CN-113403636-A | Synthetic method of alpha, beta-dichlorobenzene sulfoxide compound | 2021-05-26 |
| CN-112209651-A | Concrete accelerator and preparation method thereof | 2020-10-12 |
| CN-112209651-B | Concrete accelerator and preparation method thereof | 2020-10-12 |
| JP-6994097-B1 | Thermosetting resin and its cured product | 2020-09-23 |
| WO-2022055086-A1 | All-solid-state battery | 2020-09-09 |
| CN-114106646-A | Top-coat composition | 2020-08-31 |
| CN-114106649-A | Top-coat composition | 2020-08-31 |
| EP-3960306-A1 | Top coat composition | 2020-08-31 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 17474764 | 2007-06-05 | Spectroscopically encoded microspheres for antigen biosensing | Langmuir : the ACS journal of surfaces and colloids |
| 12940737 | 2003-09-03 | Preparation, physical properties, on-bead binding assay and spectroscopic reliability of 25 barcoded polystyrene-poly(ethylene glycol) graft copolymers | Journal of the American Chemical Society |
