369144
2-(Trifluoromethyl)acrylic acid
98%
Sinonimo/i:
TFMAA
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Cambia visualizzazione
5 G
CHF 240.00
About This Item
Formula condensata:
H2C=C(CF3)CO2H
Numero CAS:
Peso molecolare:
140.06
Numero MDL:
Codice UNSPSC:
12162002
ID PubChem:
NACRES:
NA.23
Prodotti consigliati
Saggio
98%
Punto di fusione
51-52 °C (lit.)
Stringa SMILE
OC(=O)C(=C)C(F)(F)F
InChI
1S/C4H3F3O2/c1-2(3(8)9)4(5,6)7/h1H2,(H,8,9)
VLSRKCIBHNJFHA-UHFFFAOYSA-N
Categorie correlate
Avvertenze
Danger
Indicazioni di pericolo
Classi di pericolo
Skin Corr. 1B
Codice della classe di stoccaggio
8A - Combustible corrosive hazardous materials
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
179.6 °F - closed cup
Punto d’infiammabilità (°C)
82 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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I clienti hanno visto anche
Extraction of domoic acid from seawater and urine using a resin based on 2-(trifluoromethyl) acrylic acid
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Analytica Chimica Acta, 610(1), 35-43 (2008)
Porkodi Kadhirvel et al.
Analytical and bioanalytical chemistry, 411(8), 1525-1536 (2019-02-03)
A molecularly imprinted polymer (MIP) was designed in order to allow the selective solid-phase extraction of carbamazepine (CBZ), an anticonvulsant and mood-stabilizing drug, at ultra-trace level from aqueous environmental samples. A structural analog of CBZ was selected as a dummy
Ling Zhang et al.
Nature, 557(7703), 86-91 (2018-05-04)
The formation of condensed matter typically involves a trade-off between structural order and flexibility. As the extent and directionality of interactions between atomic or molecular components increase, materials generally become more ordered but less compliant, and vice versa. Nevertheless, high
Zhengqiang Dai et al.
Journal of molecular modeling, 21(11), 290-290 (2015-10-27)
Recently, a series of computational and combinatorial approaches were employed to improve the efficiency of screening for optimal molecularly imprinted polymer (MIP) systems. In the present work, we investigated MIP systems based on enrofloxacin (ENRO) as the template molecule and
Molecularly imprinted fluorescent-shift receptors prepared with 2-(trifluoromethyl) acrylic acid
Matsui J, et al.
Analytical Chemistry, 72(14), 3286-3290 (2000)
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