Organometallic Compounds
eMolecules 5-Bromo-1H-inden-1-one | 338989-48-3 | MFCD09842501 | 250mg
Ambeed | 5-Bromo-1H-inden-1-one | 250mg | 600842194 | A516157 | | 338989-48-3 | MFCD09842501 | 209.042 | C9H5BrO
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eMolecules 2,3-Dihydro-1H-inden-5-amine | 24425-40-9 | MFCD00003803 | 1g
Oakwood Chemical | 2,3-Dihydro-1H-inden-5-amine | 1g | 537716760 | 225604 | | 24425-40-9 | MFCD00003803 | 133.194 | C9H11N
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TARGETMOL CHEMICALS INC SX-682 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. SX-682 is a potent selective and orally bioavailable inhibitor of CXCR1/2 has the potential to treat castration-resistant prostate cancer. purity: 99%
Medchemexpress LLC DBCO-PEG3-acid | 2754384-59-1 | 98.35% | 508.56 | 25 MG
DBCO-PEG3-acid is a non-cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). It contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
- Non-cleavable 3 unit PEG ADC linker
- Contains a DBCO group for strain-promoted alkyne-azide cycloaddition (SPAAC) with azide groups
- For research use only
Medchemexpress LLC Trimethoxy(4-phenylbutyl)silane | 152958-91-3 | 99.6% | 254.40 | 10 G
Trimethoxy(4-phenylbutyl)silane is a drug intermediate used for the synthesis of various active compounds. It is intended for research purposes only and not for sale to patients. This product has not been fully validated for medical applications and is for research use only.
- Drug intermediate for synthesis of various active compounds
- Purity: 99.63%
- Available in various quantities from 100 mg to 25 g
Medchemexpress LLC Trimethoxy(4-phenylbutyl)silane | 152958-91-3 | 99.63% | 254.40 | 5 G
Trimethoxy(4-phenylbutyl)silane is a drug intermediate for the synthesis of various active compounds. It is sold for research purposes only and not for patient use.
- Appearance: Liquid
- Color: Colorless to light yellow
Medchemexpress LLC Phenyl 2-bromoacetate | 620-72-4 | 99.9% | 215.04 | 25 G
Phenyl 2-bromoacetate is a biochemical reagent that can be used as a biological material or organic compound for life science-related research. It is intended for research use only and is not sold to patients.
- Biochemical reagent
- Can be used as a biological material
- Can be used as an organic compound
- Suitable for life science related research
![Medchemexpress LLC 2-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine-6-methanol | 1374639-77-6 | 99.0% | 251.72 | 100 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000404382-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine-6-methanol | 1374639-77-6 | 99.0% | 251.72 | 100 G
2-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine-6-methanol is a drug intermediate used in the synthesis of various active compounds. This product is intended for research purposes only and is not suitable for patient use.
- Drug intermediate for synthesis of various active compounds.
- Intended for research use only.
- Available in multiple quantities.
Med Vet International Exel Needle, 16G X 1in, Hypodermic, Vet Use, 100/BX, 26457
This Exel International 26457 Needle is a 16G X 1' Regular Wall needle. Regular wall needles are more rigid than thin wall needles, providing extra support and less flex due to added annula thickness. This hypodermic needle is a hollow needle used for withdrawing fluid like blood samples, or injecting medications. This quantity is 100/BX
Medchemexpress LLC Aminooxy-PEG3-acid | 1807540-79-9 | 95.0% | 237.25 | 100 MG
Aminooxy-PEG3-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Exploits the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
Medchemexpress LLC Azido-PEG5-CH2CO2-NHS | 2144777-77-3 | 97% | C16H26N4O9 | 250 MG
Azido-PEG5-CH2CO2-NHS is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It is a click chemistry reagent containing an Azide group, which allows it to undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- PEG-based PROTAC linker for synthesis
- Click chemistry reagent with azide group
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules
- Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups
Medchemexpress LLC m-PEG5-NH2 | 5498-83-9 | 99.0% | C11H25NO5 | 250 MG
m-PEG5-NH2 is a PEG-based PROTAC linker used in the synthesis of PROTACs. PROTACs are molecules consisting of two distinct ligands connected by a linker: one ligand targets an E3 ubiquitin ligase, and the other targets a specific protein. These molecules function by leveraging the intracellular ubiquitin-proteasome system to selectively degrade target proteins. This product is for research use only and not sold to patients.
- Purity: 99.02%
- Molecular weight: 251.32
- Formula: C11H25NO5
- CAS number: 5498-83-9
- Appearance: Liquid (density: 1.023±0.06 g/cm³)
- Color: Colorless to light yellow
- SMILES: COCCOCCOCCOCCOCCN
- Leverages the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
Medchemexpress LLC 4,7,10,16,19,22-Hexaoxa-13-azapentacosanedioic acid, 1,25-bis(1,1-dimethylethyl) ester | 1814901-03-5 | 98.0% | C26H51NO10 | 250 MG
NH-bis(PEG3-Boc) is a PEG-based PROTAC linker. It can be used in the synthesis of PROTACs, which are molecules designed to selectively degrade target proteins by utilizing the intracellular ubiquitin-proteasome system.
- Used in the synthesis of PROTACs.
- PROTACs contain two different ligands connected by a linker; one targets an E3 ubiquitin ligase, and the other targets the protein of interest.
- PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
Medchemexpress LLC Azido-PEG3-C3-OH | 1807512-36-2 | 98.0% | C9H19N3O4 | 250 MG
Azido-PEG3-C3-OH is a PEG-based PROTAC linker designed for use in the synthesis of PROTACs. This click chemistry reagent features an Azide group, facilitating copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. It also supports strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- PEG-based PROTAC linker
- Utilized in the synthesis of PROTACs
- Functions as a click chemistry reagent
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions