Indene - CAS 95-13-6
Catalog: |
BB041625 |
Product Name: |
Indene |
CAS: |
95-13-6 |
Synonyms: |
1H-indene |
IUPAC Name: | 1H-indene |
Description: | Indene is a useful research chemical. |
Molecular Weight: | 116.16 |
Molecular Formula: | C9H8 |
Canonical SMILES: | C1C=CC2=CC=CC=C21 |
InChI: | InChI=1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2 |
InChI Key: | YBYIRNPNPLQARY-UHFFFAOYSA-N |
Boiling Point: | 181 °C |
Melting Point: | -2°C |
Flash Point: | 58°C |
Purity: | ≥ 90% |
Density: | 0.996 g/cm3 |
Appearance: | Colorless to pale yellow liquid |
Storage: | Keep in dark place, Inert atmosphere, Store in freezer, under -20 °C |
MDL: | MFCD00003777 |
LogP: | 2.25590 |
Refractive Index: | 1.567-1.572 |
Stability: | Stable, but air and light sensitive; may polymerize upon exposure to light. Typically contains aroung 80 - 100 ppm of p-tert-butylcatechol as inhibitor. Refrigerate. Flammable. Incompatible with strong oxidizing agents. |
Vapor Pressure: | 1.1 [mmHg] |
GHS Hazard Statement: | H226 (100%): Flammable liquid and vapor [Warning Flammable liquids] |
Precautionary Statement: | P210, P233, P240, P241, P242, P243, P280, P301+P310, P303+P361+P353, P331, P370+P378, P403+P235, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
WO-2021130622-A2 | Ruthenium complex and method of conducting olefin metathesis reactions with formation of an internal bond using the ruthenium complex as a catalyst | 20191223 |
US-2021138444-A1 | Longer-Lived Ruthenium Olefin Metathesis Catalysts Supported by Hemi-Labile Carbene Ligands | 20191111 |
WO-2020191207-A1 | Therapeutic methods for treating hepatitis b | 20190320 |
WO-2020162725-A1 | Target protein eed degradation-inducing degraducer, preparation method thereof, and pharmaceutical composition for preventing or treating diseases related to eed, ezh2, or prc2, comprising same as active ingredient | 20190207 |
KR-20200097222-A | Target protein degradation inducing compound, preparation method thereof and pharmaceutical composition for preventing or treating EED, EZH2, or PRC2 related diseases containing the same as an active ingredient | 20190207 |
PMID | Publication Date | Title | Journal |
27750016 | 20170417 | Toward the Design of Less Hazardous Chemicals: Exploring Comparative Oxidative Stress in Two Common Animal Models | Chemical research in toxicology |
26731479 | 20160205 | Indenes and tetralenes analogues attenuates lipopolysaccharide-induced inflammation: An in-vitro and in-vivo study | Chemico-biological interactions |
22825321 | 20121107 | Solution-processed nickel acetate as hole collection layer for polymer solar cells | Physical chemistry chemical physics : PCCP |
23094690 | 20121102 | Synthesis of indenes via Brønsted acid catalyzed cyclization of diaryl- and alkyl aryl-1,3-dienes | Organic letters |
23001702 | 20121022 | Two-step synthesis of stable dioxadicarbaporphyrins from bis(3-indenyl)methane | Angewandte Chemie (International ed. in English) |
Complexity: | 124 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 116.062600255 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 0 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 116.062600255 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 0 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.9 |
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