Cas no 1261993-68-3 (3-(2,3-Dimethylphenyl)-5-trifluoromethylbenzoic acid)
1261993-68-3 structure
Product Name:3-(2,3-Dimethylphenyl)-5-trifluoromethylbenzoic acid
CAS No:1261993-68-3
MF:C16H13F3O2
MW:294.268435239792
MDL:MFCD18319285
CID:2621605
PubChem ID:53225215
Update Time:2025-04-21
3-(2,3-Dimethylphenyl)-5-trifluoromethylbenzoic acid Chemical and Physical Properties
Names and Identifiers
-
- 2',3'-Dimethyl-5-(trifluoromethyl)[1,1'-biphenyl]-3-carboxylic acid
- 3-(2,3-DIMETHYLPHENYL)-5-TRIFLUOROMETHYLBENZOIC ACID
- 1261993-68-3
- DTXSID40688947
- 3-(2,3-Dimethylphenyl)-5-trifluoromethylbenzoic acid, 95%
- MFCD18319285
- 3-(2,3-Dimethylphenyl)-5-trifluoromethylbenzoic acid
-
- MDL： MFCD18319285
- Inchi： 1S/C16H13F3O2/c1-9-4-3-5-14(10(9)2)11-6-12(15(20)21)8-13(7-11)16(17,18)19/h3-8H,1-2H3,(H,20,21)
- InChI Key： QDAINHLFKJVUKD-UHFFFAOYSA-N
- SMILES： FC(C1=CC(C(=O)O)=CC(=C1)C1C=CC=C(C)C=1C)(F)F
Computed Properties
- Exact Mass: 294.087
- Monoisotopic Mass: 294.087
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 21
- Rotatable Bond Count: 2
- Complexity: 380
- 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
- Topological Polar Surface Area: 37.3A^2
- XLogP3: 4.7
3-(2,3-Dimethylphenyl)-5-trifluoromethylbenzoic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB326283-5 g |
3-(2,3-Dimethylphenyl)-5-trifluoromethylbenzoic acid, 95%; . |
1261993-68-3 | 95% | 5g |
€1159.00 | 2023-04-26 | |
| abcr | AB326283-5g |
3-(2,3-Dimethylphenyl)-5-trifluoromethylbenzoic acid, 95%; . |
1261993-68-3 | 95% | 5g |
€1159.00 | 2025-04-21 |
3-(2,3-Dimethylphenyl)-5-trifluoromethylbenzoic acid Related Literature
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1. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
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Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
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