Cas no 1365969-07-8 (2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID)
2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID Chemical and Physical Properties
Names and Identifiers
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- 2-methyl-2-(trifluoromethyl)butanoic acid(WXFC0755)
- 2-methyl-2-(trifluoromethyl)butanoic acid
- 2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID
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- Inchi: 1S/C6H9F3O2/c1-3-5(2,4(10)11)6(7,8)9/h3H2,1-2H3,(H,10,11)
- InChI Key: OGQSDUJEHJTRDA-UHFFFAOYSA-N
- SMILES: C(O)(=O)C(C)(C(F)(F)F)CC
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 11
- Rotatable Bond Count: 3
2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD00963034-1g |
2-Methyl-2-(trifluoromethyl)butanoic acid |
1365969-07-8 | 97% | 1g |
¥15540.0 | 2023-04-02 |
2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID Related Literature
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Guang Xu,Wei Zhang,Ying Zhang,Xiaoxia Zhao,Ping Wen,Di Ma RSC Adv., 2018,8, 19353-19361
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Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
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Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
Additional information on 2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID
Comprehensive Overview of 2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID (CAS No. 1365969-07-8)
2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID (CAS No. 1365969-07-8) is a specialized organic compound gaining attention in pharmaceutical and agrochemical research due to its unique structural properties. The presence of a trifluoromethyl group enhances its metabolic stability and lipophilicity, making it valuable for drug design. Researchers are increasingly exploring its applications in small-molecule therapeutics and catalyst systems, aligning with trends in green chemistry and sustainable synthesis.
The compound’s sterically hindered carboxylic acid moiety allows selective reactivity, a feature leveraged in peptide coupling and bioconjugation techniques. Recent studies highlight its role in proteolysis-targeting chimeras (PROTACs), a hot topic in targeted protein degradation therapies. Its CAS No. 1365969-07-8 is frequently searched alongside terms like "fluorinated building blocks" and "high-value intermediates," reflecting industry demand for tailor-made synthons.
From a synthetic perspective, 2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID is synthesized via Grignard reactions or electrophilic trifluoromethylation, methods optimized for scalable production. Its low toxicity profile (non-GHS classified) makes it suitable for API development, addressing the growing need for safer fluorochemicals. Analytical data (NMR, HPLC) confirm >98% purity, meeting GMP standards for preclinical use.
Environmental considerations are pivotal. The compound’s persistence and bioaccumulation potential are under scrutiny, mirroring broader concerns about PFAS alternatives. Regulatory bodies emphasize readily biodegradable designs, positioning 1365969-07-8 as a candidate for eco-friendly fluorophores in imaging agents.
Market-wise, suppliers list it under custom fluorination services, catering to CRISPR-based research and mRNA vaccine adjuvants. Patent filings reveal utility in OLED materials and liquid crystals, tapping into the electronics boom. SEO-optimized queries like "CAS 1365969-07-8 supplier" or "trifluoromethylated carboxylic acid uses" reflect commercial interest.
In conclusion, 2-METHYL-2-(TRIFLUOROMETHYL)BUTANOIC ACID exemplifies innovation at the nexus of medicinal chemistry and material science. Its versatility answers pressing needs in precision medicine and clean energy technologies, ensuring sustained relevance in R&D pipelines worldwide.
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