추천 제품
분석
98%
mp
51-52 °C (lit.)
SMILES string
OC(=O)C(=C)C(F)(F)F
InChI
1S/C4H3F3O2/c1-2(3(8)9)4(5,6)7/h1H2,(H,8,9)
InChI key
VLSRKCIBHNJFHA-UHFFFAOYSA-N
애플리케이션
2-(Trifluoromethyl)acrylic acid (TFMAA) is a strong acid functional monomer, which shows a good performance in the solid-phase extraction of domoic acid. It can also be used in the preparation of molecularly imprinted polymers that show diastereoselectivity for cinchona alkaloids.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
179.6 °F - closed cup
Flash Point (°C)
82 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
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
Analytical Chemistry, 72(14), 3286-3290 (2000)
Extraction of domoic acid from seawater and urine using a resin based on 2-(trifluoromethyl) acrylic acid
Analytica Chimica Acta, 610(1), 35-43 (2008)
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
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
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