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Filtered Search Results
Aobchem (4 -(Hydroxymethyl)-[1 1 -biphenyl]-4-yl)boronic acid | 95% | CAS 1315259-16-5 | C13H13BO3 | 1g
(4 -(Hydroxymethyl)-[1 1 -biphenyl]-4-yl)boronic acid | 95% | CAS 1315259-16-5 | C13H13BO3 | 1g
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Aobchem 4-Bromo-3-(hydroxymethyl)benzonitrile | ≥95% | CAS 905710-66-9 | C8H6BrNO | 1g
4-Bromo-3-(hydroxymethyl)benzonitrile | ≥95% | CAS 905710-66-9 | C8H6BrNO | 1g
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Aobchem 2 6-Dichloro-4-(hydroxymethyl)phenol | ≥97% | CAS 22002-17-1 | C7H6Cl2O2 | 500mg
2 6-Dichloro-4-(hydroxymethyl)phenol | ≥97% | CAS 22002-17-1 | C7H6Cl2O2 | 500mg
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Aobchem 5-Hydroxymethyl-2-phenylpyridine | ≥97% | CAS 4634-09-7 | C12H11NO | 1g
5-Hydroxymethyl-2-phenylpyridine | ≥97% | CAS 4634-09-7 | C12H11NO | 1g
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eMolecules 138647-49-1 | 1-Boc-4-(trifluoromethanesulfonyloxy)-3,6-dihydro-2H-pyridine | Synthonix - Stock | MFCD09997858 | 331.310 | C11H16F3NO5S | 95.000 | CC(C)(C)OC(=O)N1CCC(OS(=O)(=O)C(F)(F)F)=CC1 | 5g | 525911277
1-Boc-4-(trifluoromethanesulfonyloxy)-3,6-dihydro-2H-pyridine | Synthonix - Stock | 138647-49-1 | MFCD09997858 | 331.310 | C11H16F3NO5S | 95.000 | CC(C)(C)OC(=O)N1CCC(OS(=O)(=O)C(F)(F)F)=CC1 | 5g | 525911277
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Medchemexpress LLC 4,7,10,13,16,19,22,25-Octaoxaheptacosanoic acid, 27-azido-, 1,1-dimethylethyl ester | 1623791-99-0 | 95.0% | 25 MG
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Azido-PEG8-Boc is a PEG- and alkyl/ether-based PROTAC linker integral to the synthesis of Proteolysis-Targeting Chimeras (PROTACs). This versatile compound also functions as a click chemistry reagent, featuring an azide group that facilitates specific bioconjugation reactions. It readily engages in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules and strain-promoted alkyne-azide cycloaddition (SPAAC) with compounds possessing DBCO or BCN groups, offering broad utility in chemical biology applications.
- PEG- and alkyl/ether-based linker
- Facilitates PROTAC synthesis
- Functions as a click chemistry reagent
- Contains an azide group for bioconjugation
- Supports copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Enables strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups
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Medchemexpress LLC N-Boc-dolaproine dicyclohexylamine | 1369427-40-6 | 99.9% | 468.67 | 500 MG
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N-Boc-dolaproine dicyclohexylamine is an amino acid residue of the pentapeptide Dolastatin 10. Dolastatin 10 inhibits tubulin polymerization and mitosis and has anticancer activity. This product also contains dicyclohexylamine and is intended for research use only.
- Inhibits tubulin polymerization
- Inhibits mitosis
- Possesses anticancer activity
- Suitable for laboratory research applications
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Medchemexpress LLC S - - -3-Boc-2 2-di 1g | 1G
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S - - -3-Boc-2 2-di 1g | 1G
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Medchemexpress LLC 1-Boc-3-(hydroxymethyl)pyrrolidine | 114214-69-6 | 98.5% | C10H19NO3 | 1 ML
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1-Boc-3-(hydroxymethyl)pyrrolidine is an intermediate used to synthesize a FGFR1/2/3/4 inhibitor (Compound 2). It is also utilized in cancer research.
- Used to synthesize a FGFR1/2/3/4 inhibitor
- Utilized in cancer research
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Medchemexpress LLC Br-Boc-C2-azido | 1120364-53-5 | >98% | 236.07 | 1 G
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Br-Boc-C2-azido is an alkyl/ether-based PROTAC linker used in the synthesis of PROTACs. It acts as a click chemistry reagent due to its Azide group, enabling participation in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules, and strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups.
- Alkyl/ether-based linker for PROTAC synthesis
- Functions as a click chemistry reagent
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Facilitates strain-promoted alkyne-azide cycloaddition (SPAAC)
- Supports PROTACs in degrading target proteins via the ubiquitin-proteasome system
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eMolecules 88950-64-5 | 1-(Boc-amino)cyclopropanecarboxylic Acid | Accela ChemBio (ASD) | MFCD00083257 | 201.222 | C9H15NO4 | 97.000 | CC(C)(C)OC(=O)NC1(CC1)C(O)=O | 0.25g | 375958232
1-(Boc-amino)cyclopropanecarboxylic Acid | Accela ChemBio (ASD) | 88950-64-5 | MFCD00083257 | 201.222 | C9H15NO4 | 97.000 | CC(C)(C)OC(=O)NC1(CC1)C(O)=O | 0.25g | 375958232
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eMolecules 286961-14-6 | N-Boc-1,2,3,6-tetrahydropyridine-4-boronic Acid Pinacol Ester | Accela ChemBio (ASD) | MFCD03840345 | 309.210 | C16H28BNO4 | 98.000 | CC(C)(C)OC(=O)N1CCC(=CC1)B1OC(C)(C)C(C)(C)O1 | 25g | 445405936
N-Boc-1,2,3,6-tetrahydropyridine-4-boronic Acid Pinacol Ester | Accela ChemBio (ASD) | 286961-14-6 | MFCD03840345 | 309.210 | C16H28BNO4 | 98.000 | CC(C)(C)OC(=O)N1CCC(=CC1)B1OC(C)(C)C(C)(C)O1 | 25g | 445405936
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Medchemexpress LLC (S)-1-Boc-3-methylpiperazine | 147081-29-6 | 100.0% | 200.28 | 1 ML
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S-1-Boc-3-methylpiperazine is a versatile drug intermediate primarily utilized in the synthesis of sotorasib. This compound is presented as a white to off-white solid, requiring specific handling and storage conditions to maintain its integrity for research applications.
- Molecular weight: 200.28
- Formula: C10H20N2O2
- CAS number: 147081-29-6
- Appearance: Solid
- Color: White to off-white
- Shipping: Room temperature in continental US; may vary elsewhere
- Storage: 4°C, protect from light; in solvent: -80°C for 6 months, -20°C for 1 month (protect from light)
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Medchemexpress LLC 3,6,9,16-Tetraoxaheptadecanoic acid, 17-phenyl-, 1,1-dimethylethyl ester | 2381196-81-0 | 95.8% | 100 MG
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Boc-C1-PEG3-C4-OBn is a PROTAC linker, which refers to the PEG composition. It can be used in the synthesis of various PROTACs. PROTACs consist of two distinct ligands linked by a linker; one ligand targets an E3 ubiquitin ligase, and the other targets the protein of interest. PROTACs leverage the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PROTAC linker with PEG composition
- Can be used in the synthesis of various PROTACs
- Targets an E3 ubiquitin ligase and a protein of interest
- Leverages the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
- For research use only
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Medchemexpress LLC Br-PEG4-CH2-Boc | 1807505-29-8 | ≥97.0% | 250 MG
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Br-PEG4-CH2-Boc is a PEG- and Alkyl/ether-based PROTAC linker that can be utilized in the synthesis of PROTACs. PROTACs are molecules designed to exploit the intracellular ubiquitin-proteasome system to selectively degrade specific target proteins.
- PEG- and alkyl/ether-based PROTAC linker
- For use in PROTAC synthesis
- PROTACs composed of two ligands connected by a linker
- Targets E3 ubiquitin ligase and target proteins
- Leverages the intracellular ubiquitin-proteasome system
- Achieves selective degradation of target proteins
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