Organometallic Compounds
Medchemexpress LLC 5-Bromo-2-trifluoromethylpyridine | 436799-32-5 | MFCD06657686 | 99.7% | C6H3BrF3N | 25 G
5-Bromo-2-trifluoromethylpyridine is a biochemical reagent primarily for life science research. It functions as a biological material or organic compound, supporting various research applications. This product is strictly for research use and not intended for patient use.
- Biochemical reagent for life science research
- Can be used as a biological material or organic compound
- Molecular weight: 225.99
- Appearance: Solid
- Color: White to off-white
- Purity: 99.7%
- For research use only
Medchemexpress LLC N-(Azido-PEG2)-N-bis(PEG4-Boc) | 2112731-81-2 | C36H70N4O14 | 250 MG
N-(Azido-PEG2)-N-bis(PEG4-Boc) is a PEG-based PROTAC linker that functions as a click chemistry reagent. It contains an Azide group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with Alkyne groups, and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups. This linker is used in the synthesis of PROTACs, which leverage the intracellular ubiquitin-proteasome system for selective degradation of target proteins.
- Used in the synthesis of PROTACs.
- Functions as a click chemistry reagent.
- Contains an Azide group, enabling CuAAc reactions with Alkyne groups and SPAAC reactions with DBCO or BCN groups.
- PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
Medchemexpress LLC Tri(amino-peg4-amide)-amine | 2523025-41-2 | 95.0% | C39H81N7O15 | 50 MG
Tri(Amino-PEG4-amide)-amine is a PEG-based PROTAC linker designed for use in the synthesis of PROTACs. It is intended for research use only and leverages the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Leverages the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
- For research use only
Cayman Chemical Tubastatin A trifluoroacetat
Potent HDAC6 inhibitor (IC50 = 15 nM) with 1,000-fold selectivity against all other HDAC isoforms (IC50s >16 μM), excluding HDAC8 (IC50 = 0.9 μM); induces α-tubulin hyperacetylation at 2.5 μM in primary cortical neuron cultures; displays dose-dependent neuronal protection of primary cortical neuron cultures at 5-10 μM
(C)C)=C/C | 250mg | 388720025](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000128446.jpg-250.jpg)
eMolecules 34880-70-1 | 1-Methoxy-1-trimethylsilyloxypropene | Combi-Blocks | MFCD00671554 | 160.288 | C7H16O2Si | 95.000 | CO\C(O[Si](C)(C)C)=C/C | 250mg | 388720025
1-Methoxy-1-trimethylsilyloxypropene | Combi-Blocks | 34880-70-1 | MFCD00671554 | 160.288 | C7H16O2Si | 95.000 | CO\C(O[Si](C)(C)C)=C/C | 250mg | 388720025
Medchemexpress LLC (S)-1-(4-(Trifluoromethoxy)phenyl)ethanamine | 951247-75-9 | 99.37% | 205.18 | 500 MG
(S)-1-(4-(Trifluoromethoxy)phenyl)ethanamine is a drug intermediate for the synthesis of various active compounds. It is for research use only and not sold to patients.
- Molecular weight: 205.18
- Formula: C9H10F3NO
- Appearance: Solid-liquid mixture
- Color: Colorless to off-white
- SMILES: FC(F)(F)OC1=CC=C([C@H](C)N)C=C1
- Purity: 99.37%
- Available documents: Data sheet, COA, SDS, HNMR, LCMS, handling instructions
- Shipping: Room temperature in continental US; may vary elsewhere
- Storage: 4°C, stored under nitrogen. In solvent: -80°C, 6 months; -20°C, 1 month (stored under nitrogen).