Cas no 30409-52-0 (3-Thiophenecarboxylicacid, 4-(9-anthracenyl)-)
30409-52-0 structure
Product Name:3-Thiophenecarboxylicacid, 4-(9-anthracenyl)-
CAS No:30409-52-0
MF:C19H12O2S
MW:304.362383842468
CID:315009
PubChem ID:315654
Update Time:2025-04-19
3-Thiophenecarboxylicacid, 4-(9-anthracenyl)- Chemical and Physical Properties
Names and Identifiers
-
- 3-Thiophenecarboxylicacid, 4-(9-anthracenyl)-
- 4-anthracen-9-ylthiophene-3-carboxylic acid
- 4-(9-Anthryl)thiophen-3-carbonsaeure
- 4-anthracen-9-yl-thiophene-3-carboxylic acid
- AC1L7S5P
- CTK1C4861
- NSC241154
- 30409-52-0
- DTXSID80311323
- NSC-241154
-
- Inchi： 1S/C19H12O2S/c20-19(21)17-11-22-10-16(17)18-14-7-3-1-5-12(14)9-13-6-2-4-8-15(13)18/h1-11H,(H,20,21)
- InChI Key： NLJOONPJBMFOKH-UHFFFAOYSA-N
- SMILES： S1C=C(C(=O)O)C(=C1)C1C2C=CC=CC=2C=C2C=CC=CC=12
Computed Properties
- Exact Mass: 304.05586
- Monoisotopic Mass: 304.056
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 22
- Rotatable Bond Count: 2
- Complexity: 402
- 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: 5.3
- Topological Polar Surface Area: 65.5?2
Experimental Properties
- Density: 1.352
- Boiling Point: 450.8°Cat760mmHg
- Flash Point: 226.4°C
- Refractive Index: 1.752
- PSA: 37.3
- LogP: 5.41970
3-Thiophenecarboxylicacid, 4-(9-anthracenyl)- Related Literature
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
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Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
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3. 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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Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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