9-Fluorenylmethanol - ≥99% , CAS No.24324-17-2

CAS: 24324-17-2 Cat. No.: F100526 Molecular Weight: 196.24 Beilstein Registry Number: 2330017 EC Number: 246-167-5

GRADE & PURITY ≥99%

Synonyms

XXSCONYSQQLHTH-UHFFFAOYSA- | 9H-fluorene-9-ylmethanol | A817227 | EN300-185373 | benzyl(tributyl)azanium;bromide | 9-Fluorenyl Methanol | ChemDiv3_002715 | Fmoc-OH 9-Fluorenylmethanol | (3aR,4S,5R,6aS)-[1,1'-Biphenyl]-4-carboxylic acid, hexahydro-4-(metho

Storage

Desiccated,Room temperature

Shipped In

Normal

Overview

Product Application：

9-Fluorenylmethanol acts as a N-protecting reagent, which is used in the synthesis of peptide. It is also used in the preparation of deoxynucleoside 9-fluorenemethyl phosphorodithioates. Further, it is used to prepare 9-(fluoromethyl)fluorene. In addition to this, it is involved in the electropolymerization with boron trifluoride diethyl etherate to yield low-potential electrodeposition of semiconducting poly(9-fluorenemethanol) film.

Specifications

Synonyms

XXSCONYSQQLHTH-UHFFFAOYSA- | 9H-fluorene-9-ylmethanol | A817227 | EN300-185373 | benzyl(tributyl)azanium;bromide | 9-Fluorenyl Methanol | ChemDiv3_002715 | Fmoc-OH 9-Fluorenylmethanol | (3aR, 4S, 5R, 6aS)-[1, 1'-Biphenyl]-4-carboxylic acid, hexahydro-4-(metho

Specifications & Purity

≥99%

Storage

Desiccated, Room temperature

Shipped In

Normal

Purity

≥99%

Names and Identifiers

• Pubchem Sid: 488186623
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488186623
• Canonical Smiles: C1=CC=C2C(=C1)C(C3=CC=CC=C32)CO
• IUPAC Name: 9H-fluoren-9-ylmethanol
• InChIKey: XXSCONYSQQLHTH-UHFFFAOYSA-N
• 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
• Isomeric SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)CO
• WGK Germany: 3
• Molecular Weight: 196.24
• Beilstein: 2330017
• Reaxy-Rn: 2330017
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2330017&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Fluorenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Fluorenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorenes
• Alternative Parents: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Fluorene - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as fluorenes. These are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in methanol.
• Melt Point(°C): 104-106°C
• Molecular Weight: 196.240 g/mol
• XLogP3: 2.700
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 196.089 Da
• Monoisotopic Mass: 196.089 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 203.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Xinhui Wang, Yuequan Wang, Jiaxin Yu, Qian Qiu, Rui Liao, Shenwu Zhang, Cong Luo.  (2023)  Reduction-Hypersensitive Podophyllotoxin Prodrug Self-Assembled Nanoparticles for Cancer Treatment.  Pharmaceutics,  15  (3): (784).  [PMID:36986645] [10.3390/pharmaceutics15030784]