Cas no 17674-16-7 (Benzyl trifluoromethanesulfonate)
Benzyl trifluoromethanesulfonate Chemical and Physical Properties
Names and Identifiers
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- Benzyl trifluoromethanesulfonate
- Methanesulfonic acid,1,1,1-trifluoro-,phenylmethyl ester
- A900990
- Methanesulfonic acid, 1,1,1-trifluoro-, phenylmethyl ester
- 1,1,1-Trifluoro-methanesulfonic acid phenylmethyl ester
- 17674-16-7
- F17014
- MFCD16036377
- DTXSID70455109
- benzyl triflate
- SCHEMBL777315
- 1,1,1-Trifluoro-methanesulfonicacidphenylmethylester
- Methanesulfonic acid, trifluoro-, phenylmethyl ester
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- Inchi： 1S/C8H7F3O3S/c9-8(10,11)15(12,13)14-6-7-4-2-1-3-5-7/h1-5H,6H2
- InChI Key： QHTRLHAGKRCHKW-UHFFFAOYSA-N
- SMILES： S(C(F)(F)F)(=O)(=O)OCC1C=CC=CC=1
Computed Properties
- Exact Mass: 240.00681
- Monoisotopic Mass: 240.00679974g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 15
- Rotatable Bond Count: 4
- Complexity: 285
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.4
- Topological Polar Surface Area: 51.8?2
Experimental Properties
- PSA: 43.37
Benzyl trifluoromethanesulfonate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-GU840-200mg |
Benzyl trifluoromethanesulfonate |
17674-16-7 | 98+% | 200mg |
874.0CNY | 2021-07-09 | |
| Ambeed | A989608-1g |
1,1,1-Trifluoro-methanesulfonic acid phenylmethyl ester |
17674-16-7 | 98% | 1g |
$354.0 | 2024-04-22 |
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Benzyl trifluoromethanesulfonate Related Literature
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
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Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
Additional information on Benzyl trifluoromethanesulfonate
Comprehensive Overview of Benzyl trifluoromethanesulfonate (CAS No. 17674-16-7): Properties, Applications, and Industry Insights
Benzyl trifluoromethanesulfonate (CAS No. 17674-16-7), often referred to as benzyl triflate, is a highly versatile organosulfur compound widely utilized in organic synthesis and pharmaceutical research. Its molecular formula, C8H7F3O3S, highlights its unique structure, combining a benzyl group with a trifluoromethanesulfonate moiety. This compound is particularly valued for its role as a alkylating agent and electrophilic reagent, making it indispensable in modern chemical laboratories.
The growing interest in Benzyl trifluoromethanesulfonate is evident from its frequent mentions in academic publications and patent filings. Researchers often search for "benzyl triflate synthesis" or "CAS 17674-16-7 applications," reflecting its relevance in peptide coupling, catalysis, and material science. Its compatibility with green chemistry principles has also sparked discussions, as industries seek sustainable alternatives for traditional reagents.
One of the standout features of Benzyl trifluoromethanesulfonate is its stability under ambient conditions, which simplifies storage and handling. Unlike some reactive intermediates, it offers a balance between reactivity and safety, a topic frequently explored in forums discussing "safe handling of benzyl triflate." This characteristic, combined with its high yield efficiency, positions it as a preferred choice for multi-step synthetic routes.
In the pharmaceutical sector, Benzyl trifluoromethanesulfonate is often employed in the protection-deprotection of functional groups, a critical step in API manufacturing. Recent studies have highlighted its utility in asymmetric synthesis, addressing the demand for chiral building blocks. These advancements align with trending searches like "triflate reagents in drug discovery" and "CAS 17674-16-7 mechanism," underscoring its interdisciplinary importance.
From an industrial perspective, the scalability of Benzyl trifluoromethanesulfonate production has been optimized to meet global demand. Manufacturers emphasize its low impurity profile, a key factor for compliance with GMP standards. Discussions on platforms like ResearchGate often focus on "bulk benzyl triflate suppliers" or "cost-effective triflation methods," reflecting its commercial viability.
Emerging applications in polymer chemistry further expand the compound’s utility. For instance, its role in cationic polymerization has been explored for designing high-performance materials. Such innovations resonate with searches like "benzyl triflate in material science" and "advanced triflate derivatives," showcasing its adaptability beyond traditional organic synthesis.
Environmental considerations are another hotspot. The compound’s biodegradability potential and low toxicity are frequently compared to conventional sulfonates in "eco-friendly reagent comparisons." This aligns with the broader shift toward sustainable chemical practices, a dominant theme in contemporary research.
In summary, Benzyl trifluoromethanesulfonate (CAS No. 17674-16-7) exemplifies innovation in synthetic chemistry. Its multifaceted applications—from pharmaceutical intermediates to advanced material design—coupled with its alignment with sustainability goals, ensure its continued prominence. As research evolves, queries like "future trends for benzyl triflate" will likely drive further exploration of this remarkable compound.
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