1H-Pyrrolo[2,3-f]quinoline - CAS 233-36-3
Catalog: |
BB018010 |
Product Name: |
1H-Pyrrolo[2,3-f]quinoline |
CAS: |
233-36-3 |
Synonyms: |
6H-pyrrolo[2,3-f]quinoline |
IUPAC Name: | 6H-pyrrolo[2,3-f]quinoline |
Description: | 1H-Pyrrolo[2,3-f]quinoline (CAS# 233-36-3) is a useful research chemical. |
Molecular Weight: | 168.19 |
Molecular Formula: | C11H8N2 |
Canonical SMILES: | C1=CNC2=CC=C3C=CN=C3C2=C1 |
InChI: | InChI=1S/C11H8N2/c1-2-9-10(12-6-1)4-3-8-5-7-13-11(8)9/h1-7,12H |
InChI Key: | NJBMMMJOXRZENQ-UHFFFAOYSA-N |
Appearance: | White to tan solid, powder, crystals, crystalline powder and/or chunks |
LogP: | 2.71610 |
GHS Hazard Statement: | H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113149912-A | Cycloalkanepyrimidine derivative and preparation method and application thereof | 20210401 |
CN-113004290-A | Organic compound, organic electroluminescent material and application thereof | 20210224 |
CN-112375002-A | 2,4, 7-trisubstituted fluorene compound and electronic device thereof | 20210118 |
CN-112375002-B | 2,4, 7-trisubstituted fluorene compound and electronic device thereof | 20210118 |
KR-20200129083-A | Compound and organic light emitting device comprising the same | 20201110 |
PMID | Publication Date | Title | Journal |
22319256 | 20111201 | Anxiolytic activity of pyridoindole derivatives SMe1EC2 and SMe1M2: behavioral analysis using rat model | Interdisciplinary toxicology |
22313311 | 20111101 | Novel hexahydropyridoindole derivative as prospective agent against oxidative damage in pancreatic β cells | Medicinal chemistry (Shariqah (United Arab Emirates)) |
21235493 | 20110701 | Effects of a long-term treatment with an antioxidant pyridoindole on vascular responsiveness in diabetes-induced aging rats | Current aging science |
21577284 | 20110301 | Safety assessment of the pyridoindole derivative SMe1EC2: developmental neurotoxicity study in rats | Interdisciplinary toxicology |
21577286 | 20110301 | The new pyridoindole antioxidant SMe1EC2 and its intervention in hypoxia/hypoglycemia-induced impairment of longterm potentiation in rat hippocampus | Interdisciplinary toxicology |
Complexity: | 443 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 168.068748264 |
Formal Charge: | 0 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 168.068748264 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 24.4 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.7 |
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