![5-[3,5-Bis(trifluoromethyl)phenyl]-1H-tetrazole (CAS 175205-09-1) - chemical structure image](https://media.scbt.com/product/5-3-5-bis-trifluoromethyl-phenyl-1h-tetrazole-175205-09-1-structure_15_36_b_153632.jpg)
![5-[3,5-Bis(trifluoromethyl)phenyl]-1H-tetrazole (CAS 175205-09-1) - chemical structure image](https://media.scbt.com/product/5-3-5-bis-trifluoromethyl-phenyl-1h-tetrazole-175205-09-1-structure_15_36_t_153632.jpg "Molecular structure of 5-[3,5-Bis(trifluoromethyl)phenyl]-1H-tetrazole, CAS Number: 175205-09-1")
Molecular structure of 5-[3,5-Bis(trifluoromethyl)phenyl]-1H-tetrazole, CAS Number: 175205-09-1
5-[3,5-Bis(trifluoromethyl)phenyl]-1H-tetrazole (CAS 175205-09-1)
Alternate Names:
1,3-Bis(trifluoromethyl)-5-(1H-tetrazol-5-yl)benzene
CAS Number:
175205-09-1
Molecular Weight:
282.15
Molecular Formula:
C9H4F6N4
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
5-[3,5-Bis(trifluoromethyl)phenyl]-1H-tetrazole is a chemical compound with a tetrazole ring structure substituted with a 3,5-bis(trifluoromethyl)phenyl group. Solutions containing 5-(3,5-bis(trifluoromethyl)phenyl)-1H-tetrazole in acetonitrile, are mixed with solutions of phosphoramidites. The activator reacts with the amidite group to form a highly reactive intermediate.
5-[3,5-Bis(trifluoromethyl)phenyl]-1H-tetrazole (CAS 175205-09-1) References
- Synthesis of branched oligonucleotides with three different sequences using an oxidatively removable tritylthio group. | Utagawa, E., et al. 2007. J Org Chem. 72: 8259-66. PMID: 17900140
- Free-radical ring closure to conformationally locked α-L-carba-LNAs and synthesis of their oligos: nuclease stability, target RNA specificity, and elicitation of RNase H. | Li, Q., et al. 2010. J Org Chem. 75: 6122-40. PMID: 20738147
- Design, synthesis, and properties of boat-shaped glucopyranosyl nucleic acid. | Mori, K., et al. 2011. Org Lett. 13: 6050-3. PMID: 22004054
- Synthesis and properties of a bridged nucleic acid with a perhydro-1,2-oxazin-3-one ring. | Shrestha, AR., et al. 2011. J Org Chem. 76: 9891-9. PMID: 22059648
- Synthesis and properties of cationic 2'-O-[N-(4-aminobutyl)carbamoyl] modified oligonucleotides. | Seio, K., et al. 2012. Bioorg Med Chem Lett. 22: 2470-3. PMID: 22406150
- Synthesis and biophysical properties of C5-functionalized LNA (locked nucleic acid). | Kumar, P., et al. 2014. J Org Chem. 79: 5047-61. PMID: 24825249
- Synthesis, hybridization characteristics, and fluorescence properties of oligonucleotides modified with nucleobase-functionalized locked nucleic acid adenosine and cytidine monomers. | Kaura, M., et al. 2014. J Org Chem. 79: 6256-68. PMID: 24933409
- Synthesis and hybridization property of a boat-shaped pyranosyl nucleic acid containing an exocyclic methylene group in the sugar moiety. | Mori, K., et al. 2015. Bioorg Med Chem. 23: 33-7. PMID: 25496806
- Recognition of Double-Stranded DNA Using Energetically Activated Duplexes Modified with N2'-Pyrene-, Perylene-, or Coronene-Functionalized 2'-N-Methyl-2'-amino-DNA Monomers. | Anderson, BA., et al. 2015. J Org Chem. 80: 5395-406. PMID: 25984765
- Photolithographic Synthesis of High-Density DNA and RNA Arrays on Flexible, Transparent, and Easily Subdivided Plastic Substrates. | Holden, MT., et al. 2015. Anal Chem. 87: 11420-8. PMID: 26494264
- Merging Two Strategies for Mixed-Sequence Recognition of Double-Stranded DNA: Pseudocomplementary Invader Probes. | Anderson, BA. and Hrdlicka, PJ. 2016. J Org Chem. 81: 3335-46. PMID: 26998918
- Hybridization and Mismatch Discrimination Abilities of 2',4'-Bridged Nucleic Acids Bearing 2-Thiothymine or 2-Selenothymine Nucleobase. | Habuchi, T., et al. 2019. J Org Chem. 84: 1430-1439. PMID: 30632750
- Effective syntheses of 2',4'-BNANC monomers bearing adenine, guanine, thymine, and 5-methylcytosine, and the properties of oligonucleotides fully modified with 2',4'-BNANC. | Fujisaka, A., et al. 2019. Bioorg Med Chem. 27: 1728-1741. PMID: 30862430
- 2',4'-BNA/LNA with 9-(2-Aminoethoxy)-1,3-diaza-2-oxophenoxazine Efficiently Forms Duplexes and Has Enhanced Enzymatic Resistance*. | Kishimoto, Y., et al. 2021. Chemistry. 27: 2427-2438. PMID: 33280173
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
5-[3,5-Bis(trifluoromethyl)phenyl]-1H-tetrazole, 5 g | sc-256880 | 5 g | $315.00 | |||
5-[3,5-Bis(trifluoromethyl)phenyl]-1H-tetrazole, 25 g | sc-256880A | 25 g | $1319.00 |