产品名称
3,3,3-三氟丙酸, 98%
InChI
1S/C3H3F3O2/c4-3(5,6)1-2(7)8/h1H2,(H,7,8)
SMILES string
OC(=O)CC(F)(F)F
InChI key
KSNKQSPJFRQSEI-UHFFFAOYSA-N
assay
98%
refractive index
n20/D 1.333 (lit.)
bp
145 °C/746 mmHg (lit.)
mp
9.7 °C (lit.)
density
1.45 g/mL at 25 °C (lit.)
functional group
carboxylic acid
fluoro
Quality Level
Application
3,3,3-三氟丙酸可用于合成：
- 2,2,2-三氟乙基3,3,3-三氟丙酸酯
- 3,3,3-三氟丙酸乙酯
- N-三氟丙酰基-D-甘露糖胺
- 3,3,3-三氟丙酰氯
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
198.0 °F - closed cup
flash_point_c
92.22 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
157 nm Resist Materials: A Progress Report.
Chiba T, et al.
J. Photopolym. Sci. Technol., 13(4), 657-664 (2000)
Synthesis of ethyl 3,3,3-trifluoropropionate from 2-bromo-3,3,3-trifluoropropene.
Inoue M, et al.
Journal of Fluorine Chemistry, 167, 135-138 (2014)
Bi-phobic cellulose fibers derivatives via surface trifluoropropanoylation.
Cunha AG, et al.
Langmuir, 23(21), 10801-10806 (2007)
Yanbin Pan et al.
Carbohydrate research, 339(12), 2091-2100 (2004-07-29)
N-Acetyl-D-neuraminic acid (NeuNAc) aldolase is an important enzyme for the metabolic engineering of cell-surface NeuNAc using chemically modified D-mannosamines. To explore the optimal substrates for this application, eight N-acyl derivatives of D-mannosamine were prepared, and their accessibility to NeuNAc aldolase
Bifan Chen et al.
Analytical chemistry, 91(18), 11661-11669 (2019-08-24)
Antibody-drug conjugates (ADCs) are designed to combine the target specificity of monoclonal antibodies and potent cytotoxin drugs to achieve better therapeutic outcomes. Comprehensive evaluation of the quality attributes of ADCs is critical for drug development but remains challenging due to
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