1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone
CAS No. 1190865-44-1
1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone( —— )
Catalog No. M28867 CAS No. 1190865-44-1
1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone is an intermediate of Sarolaner.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 29 | In Stock |
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| 25MG | 51 | In Stock |
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| 50MG | 75 | In Stock |
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| 100MG | 112 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 276 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product Name1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone
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NoteResearch use only, not for human use.
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Brief Description1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone is an intermediate of Sarolaner.
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Description1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone is an intermediate of Sarolaner.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorPKC-ι
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Research Area——
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Indication——
Chemical Information
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CAS Number1190865-44-1
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Formula Weight261
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Molecular FormulaC8H2Cl2F4O
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Purity>98% (HPLC)
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Solubility——
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SMILESFc1c(Cl)cc(cc1Cl)C(=O)C(F)(F)F
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Cyclo(Pro-Gly)
Cyclo(Pro-Gly) is an active metabolite of piracetam-N-phenylacetyl-L-prolylglycine (GWS-111), it shows a greater resistance to an enzymatic effect than natural neuropeptides. Cyclo-(Gly-Pro) shows cytotoxicity at the concentration of 10 umol/L, it inhibits the growth of Bacillus subtilis with the minimal inhibitory concentration (MIC) value of 0.8, 0.8 g/L.
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Interiorin
Interiorin can be isolated from Kadsura heteroclita and has moderate anti-HIV activity with an EC50 value of 1.6 lg/mL.
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[Sar1, Ile8]-Angiote...
[Sar1, Ile8]-Angiotensin II is a peptide that has multiple effects on vascular smooth muscle, including contraction of normal arteries and hypertrophy or hyperplasia of cultured cells or diseased vessels. The biological activities of angiotensin II antagonists upon basal and angiotensin II-stimulated aldosterone production were evaluated in an isolated canine glomerulosa cell preparation.
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