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Merck
CN

329398

Trifluorothymidine

99%

Synonym(s):

α,α,α-Trifluorothymidine, 2′-Deoxy-5-trifluoromethyluridine, Trifluorothymine deoxyriboside, Trifluridine

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About This Item

Empirical Formula (Hill Notation):
C10H11F3N2O5
CAS Number:
Molecular Weight:
296.20
EC Number:
200-722-8
UNSPSC Code:
12352200
MDL number:
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InChI key

VSQQQLOSPVPRAZ-RRKCRQDMSA-N

InChI

1S/C10H11F3N2O5/c11-10(12,13)4-2-15(9(19)14-8(4)18)7-1-5(17)6(3-16)20-7/h2,5-7,16-17H,1,3H2,(H,14,18,19)/t5-,6+,7+/m0/s1

SMILES string

OC[C@H]1O[C@H](C[C@@H]1O)N2C=C(C(=O)NC2=O)C(F)(F)F

assay

99%

mp

190-193 °C (lit.)

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P Mellado-García et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 86, 365-373 (2015-11-27)
Essential oils from onion (Allium cepa L.), garlic (Allium sativum L.), and their main components, such as propyl thiosulfinate oxide (PTSO) are being intended for active packaging with the purpose of maintaining and extending food product quality and shelf life.
Kana Nishihara et al.
Mutagenesis, 31(1), 69-81 (2015-08-06)
DNA repair pathways play a critical role in maintaining cellular homeostasis by repairing DNA damage induced by endogenous processes and xenobiotics, including environmental chemicals. Induction of DNA damage may lead to genomic instability, disruption of cellular homeostasis and potentially tumours.

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