9-Fluorenylmethanol - CAS 24324-17-2
Catalog: |
BB018415 |
Product Name: |
9-Fluorenylmethanol |
CAS: |
24324-17-2 |
Synonyms: |
Fmoc-OH; Fluorene-9-methanol; (9H-Fluoren-9-yl)methanol; 9-(Hydroxymethyl)fluorene; 9-Fluorenylmethanol; 9-Fluorenylmethyl Alcohol; 9H-Fluorene-9-methanol; 9-Hydroxymethylfluorene; fluoren-9-ylmethan-1-ol; (9h-fluoren-9-yl)methanol; hofm |
IUPAC Name: | 9H-fluoren-9-ylmethanol |
Description: | 9-Fluorenemethanol is used in the design and in the synthesis of novel type somatostatin analogs with antiproliferative activities on A431 tumor cells. |
Molecular Weight: | 196.24 |
Molecular Formula: | C14H12O |
Canonical SMILES: | C1=CC=C2C(=C1)C(C3=CC=CC=C32)CO |
InChI: | InChI=1S/C14H12O/c15-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14-15H,9H2 |
InChI Key: | XXSCONYSQQLHTH-UHFFFAOYSA-N |
Boiling Point: | 293.1 ℃ (Predicted) |
Melting Point: | 105-107 ℃ |
Purity: | ≥ 99 % (HPLC) |
Density: | 1.030 g/cm3 (Predicted) |
Solubility: | Slightly soluble in Chloroform, Methanol |
Appearance: | White to light yellowish crystalline powder |
Storage: | Store at 2-8 ℃ |
MDL: | MFCD00001139 |
LogP: | 2.79120 |
Publication Number | Title | Priority Date |
CN-113354514-A | Method for controllable high-selectivity synthesis of 9-fluorenylmethanol and 9, 9-bis (hydroxymethyl) fluorene | 20210607 |
CN-113150075-A | Novel cyclic poly-arginine membrane-penetrating peptide molecule and synthesis method and application thereof | 20210514 |
CN-113159449-A | Structured data-based prediction method | 20210513 |
CN-113159450-A | Prediction system based on structured data | 20210513 |
CN-113191441-A | Adaptive relation modeling method for structured data | 20210513 |
PMID | Publication Date | Title | Journal |
22726928 | 20120715 | Synthesis of nucleoside 5'-boranophosphorothioate derivatives using an H-boranophosphonate monoester as a precursor | Bioorganic & medicinal chemistry letters |
21731544 | 20110101 | Marine biocatalysts: enzymatic features and applications | Marine drugs |
20886937 | 20100928 | High resolution electronic spectroscopy of 9-fluorenemethanol in the gas phase: new insights into the properties of Π-hydrogen bonds | The Journal of chemical physics |
18576391 | 20080901 | Facile biocatalytic access to 9-fluorenylmethyl polyglycosides: evaluation of antiviral activity on immunocompetent cells | ChemMedChem |
18481049 | 20080701 | Ultratrace-level determination of glyphosate, aminomethylphosphonic acid and glufosinate in natural waters by solid-phase extraction followed by liquid chromatography-tandem mass spectrometry: performance tuning of derivatization, enrichment and detection | Analytical and bioanalytical chemistry |
Complexity: | 203 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 196.088815002 |
Formal Charge: | 0 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 196.088815002 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 20.2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.7 |
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