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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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B107656-5g
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5g |
6
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$36.90
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B107656-25g
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25g |
4
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$108.90
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B107656-100g
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100g |
5
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$232.90
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B107656-500g
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500g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
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$1,047.90
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| Synonyms | J2DF3P68J2 | Q-101150 | SY004751 | BCP27073 | SCHEMBL415882 | 2-Bromo-9H-fluorene # | MFCD00001115 | EINECS 214-480-6 | AKOS015835445 | 9H-Fluorene,2-bromo | AM20060920 | 9H-Fluorene, 2-bromo- | DTXSID00150357 | FT-0611561 | 2-BROMO-9H-FLUORENE | 2-Bromof |
|---|---|
| Specifications & Purity | ≥97% |
| Biochemical and Physiological Mechanisms | Employed in a study of the conversion of aryl bromides to aryltriethoxysilanes via a Barbier-type reaction using ultrasound irradiation. Also used in the preparation of N-carbazole end-capped oligofluorenes. |
| Shipped In | Normal |
| Product Description |
Usually used in the synthesis of end-capping reagent 2-bromo-9,9-di-nhexylfluorene, the synthesis of 2-bromo-9,9-dihexylfluorene;also has been used in the preparation of poly(di-n-hexylfluorene)s end capped with 2-bromofluorene, 2-bromo-9,9-di-n-hexylfluorene and 9-bromoanthracene through Ni(0) mediated polymerization. product description: 2-Bromofluorene is a nonintrusive end-capping reagent to control molecular weights and to generate well-defined oligomers. application: 2-Bromofluorene was used in the synthesis of end-capping reagent 2-bromo-9,9-di-nhexylfluorene. It has been used in the preparation of poly(di-n-hexylfluorene)s end capped with 2-bromofluorene, 2-bromo-9,9-di-n-hexylfluorene and 9-bromoanthracene through Ni(0) mediated polymerization. It was also used in the synthesis of 2-bromo-9,9-dihexylfluorene. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Fluorenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fluorenes |
| Alternative Parents | Aryl bromides Organobromides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Fluorene - Aryl halide - Aryl bromide - Hydrocarbon derivative - Organobromide - Organohalogen compound - 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 |
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| Pubchem Sid | 504752553 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752553 |
| IUPAC Name | 2-bromo-9H-fluorene |
| INCHI | InChI=1S/C13H9Br/c14-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8H,7H2 |
| InChIKey | FXSCJZNMWILAJO-UHFFFAOYSA-N |
| Smiles | C1C2=CC=CC=C2C3=C1C=C(C=C3)Br |
| Isomeric SMILES | C1C2=CC=CC=C2C3=C1C=C(C=C3)Br |
| WGK Germany | 3 |
| Molecular Weight | 245.11 |
| Beilstein | 5(4)2147 |
| Reaxy-Rn | 1946701 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1946701&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jul 01, 2025 | B107656 | |
| Certificate of Analysis | Feb 11, 2025 | B107656 | |
| Certificate of Analysis | Apr 27, 2024 | B107656 | |
| Certificate of Analysis | Apr 27, 2024 | B107656 | |
| Certificate of Analysis | Apr 27, 2024 | B107656 | |
| Certificate of Analysis | Oct 13, 2023 | B107656 | |
| Certificate of Analysis | Oct 13, 2023 | B107656 | |
| Certificate of Analysis | Oct 13, 2023 | B107656 | |
| Certificate of Analysis | Oct 13, 2023 | B107656 | |
| Certificate of Analysis | May 09, 2023 | B107656 | |
| Certificate of Analysis | Dec 12, 2022 | B107656 | |
| Certificate of Analysis | Dec 12, 2022 | B107656 | |
| Certificate of Analysis | Dec 12, 2022 | B107656 | |
| Certificate of Analysis | Dec 12, 2022 | B107656 | |
| Certificate of Analysis | Jan 19, 2022 | B107656 |
| Solubility | Soluble in Toluene |
|---|---|
| Boil Point(°C) | 185°C/135mmHg |
| Melt Point(°C) | 114°C |
| Molecular Weight | 245.110 g/mol |
| XLogP3 | 4.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 243.989 Da |
| Monoisotopic Mass | 243.989 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 213.000 |
| 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 |
| 1. Liandong Ye, Min Liu, Xiao Wang, Zhihong Yu, Zhihao Huang, Nianchen Zhou, Zhengbiao Zhang, Xiulin Zhu. (2023) Sequence effect on the self-assembly of discrete amphiphilic co-oligomers with fluorene-azobenzene semirigid backbones. RSC Advances, 13 (35): (24181-24190). |
| 2. Yin Zhao, Hailing Chen, Lu Yin, Xiaoxiao Cheng, Wei Zhang, Xiulin Zhu. (2018) Chirality induction of achiral polydialkylfluorenes by chiral solvation: odd–even and side chain length dependence. Polymer Chemistry, 9 (17): (2295-2301). |
| 3. Wenxiu Yao, Pengfei Wu, Yidan Xie, Xinyu Shen, Shuwei Xia, Liangmin Yu. (2024) Synthesis and photophysical properties of charge transfer cocrystals based on TCNB and fluorene and its derivatives. CRYSTENGCOMM, |