Organo-Metalloid Compounds
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Filtered Search Results
Aobchem AOBCHEM
5001059969 TETRAETHYL DIMETHYLAMINO MET
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eMolecules 2247367-07-1 | 4,4,5,5-tetraethyl-2-(4,4,5,5-tetraethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane | Pharmablock366.160 | C20H40B2O4 | 97.000 | CCC1(CC)OB(OC1(CC)CC)B1OC(CC)(CC)C(CC)(CC)O1 | 5g | 783662447
4,4,5,5-tetraethyl-2-(4,4,5,5-tetraethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane | Pharmablock | 2247367-07-1366.160 | C20H40B2O4 | 97.000 | CCC1(CC)OB(OC1(CC)CC)B1OC(CC)(CC)C(CC)(CC)O1 | 5g | 783662447
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eMolecules 2247367-07-1 | 4,4,5,5-tetraethyl-2-(4,4,5,5-tetraethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane | Pharmablock366.160 | C20H40B2O4 | 97.000 | CCC1(CC)OB(OC1(CC)CC)B1OC(CC)(CC)C(CC)(CC)O1 | 25g | 783664274
4,4,5,5-tetraethyl-2-(4,4,5,5-tetraethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane | Pharmablock | 2247367-07-1366.160 | C20H40B2O4 | 97.000 | CCC1(CC)OB(OC1(CC)CC)B1OC(CC)(CC)C(CC)(CC)O1 | 25g | 783664274
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Medchemexpress LLC TFP-PEG3-TFP 50mg
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TFP-PEG3-TFP is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]
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Medchemexpress LLC Azido-peg3-dykddddk tfa | 1242.20 | 5 MG
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Azido-PEG3-DYKDDDDK (azide-PEG3-FLAG) TFA is a multifunctional fusion tag used for the purification of recombinant proteins. This click chemistry reagent contains an azide group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with molecules containing alkyne groups. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- Multifunctional fusion tag for the purification of recombinant proteins
- Contains an azide group
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with molecules containing alkyne groups
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups
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Medchemexpress LLC m-PEG3-CH2CH2COOH | 67319-28-2 | MFCD11041124 | 97.0% | 236.26 g·mol⁻¹ | C10H20O6 | 5 G
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m-PEG3-CH2CH2COOH is a methoxy-terminated PEG3 carboxylic acid used as a short, flexible spacer for bioconjugation chemistry. It is employed as a non-cleavable linker in antibody-drug conjugate (ADC) assembly and as a PEG-based linker in PROTAC and other conjugation workflows, providing a terminal carboxylic acid for coupling reactions and improving solubility of conjugates.
- Methoxy-terminated PEG3 spacer providing flexibility.
- Terminal carboxylic acid suitable for amide coupling and esterification.
- Molecular weight 236.26 g·mol⁻¹ for predictable spacer length.
- High purity (approximately 97.0%) suitable for research applications.
- Available in small research-scale quantities and recommended refrigerated storage for stability.
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Medchemexpress LLC BCN-exo-PEG3-NH2 | 1841134-72-2 | 99.9% | 368.47 | 250 MG
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BCN-exo-PEG3-NH2 is a PEG-based PROTAC linker primarily used in the synthesis of PROTACs. It acts as a click chemistry reagent, featuring a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing azide groups. PROTACs leverage the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- Purity: 99.94%
- Molecular weight: 368.47
- Chemical formula: C19H32N2O5
- CAS number: 1841134-72-2
- Appearance: Colorless to light yellow liquid
- Density: 1.14±0.1 g/cm3
- Used in PROTAC synthesis
- Contains a BCN group for SPAAC reactions
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Medchemexpress LLC N-Boc-PEG5-bromide | 1392499-32-9 | MFCD31536756 | 98.0% | 400.31 g·mol⁻¹ | C15H30BrNO6 | 100 MG
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N-Boc-PEG5-bromide is a Boc-protected polyethylene glycol (PEG) linker bearing a terminal bromide functional group. It is used as a reactive building block in the synthesis of antibody-drug conjugates (ADCs) and PROTACs to introduce a five-unit PEG spacer that improves solubility and provides a reactive handle for conjugation chemistry.
- Boc-protected amine allows selective deprotection under acidic conditions.
- Terminal bromide enables alkylation and nucleophilic substitution reactions.
- Five-unit PEG spacer improves aqueous solubility and linker flexibility.
- High purity suitable for research applications (98.0%).
- Supplied as a solid and available in small-scale pack sizes including 100 MG.
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Medchemexpress LLC Nh2-peg3 (protac linker 35) | 6338-55-2 | MFCD07367495 | 149.19 | 1 G
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NH2-PEG3 (PROTAC Linker 35) is a PROTAC linker, which belongs to a polyethylene glycol (PEG) linker. This compound can be used in the synthesis of the PROTAC (β-NF-JQ1).
- PROTAC linker
- Polyethylene glycol (PEG) linker
- Suitable for synthesis of PROTAC (β-NF-JQ1)
- Colorless to light yellow liquid
- Purity: 99.87%
- Molecular weight: 149.19
- CAS number: 6338-55-2
- Density: 1.0773 g/cm3
- Solubility in DMSO: 100 mg/mL
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Medchemexpress LLC Atorvastatin-PEG3-FITC | 1440755-31-6 | 98.2% | C64H68FN5O12S | 10MG
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Atorvastatin-PEG3-FITC is a fluorescently labeled derivative of atorvastatin used as a ligand in fluorescence anisotropy assays and reported as a KRAS-PDEδ interaction inhibitor (compound S31). It is provided for research use with defined chemical characteristics and high reported purity suitable for biochemical experiments.
- Acts as a ligand in fluorescence anisotropy assays.
- Reported to inhibit KRAS-PDEδ interaction (compound S31).
- Contains an FITC fluorescent tag for fluorescence-based detection.
- High reported purity (98.17%) suitable for biochemical assays.
- Defined molecular formula and molecular weight for assay calculations.
- Available in small research pack sizes for assay optimization.
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Medchemexpress LLC Dbco-nhco-peg3-fmoc | 00-00-0 | 96.9% | C42H43N3O7 | 10MG
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DBCO-NHCO-PEG3-Fmoc is a DBCO-functionalized PEG3 linker with an Fmoc-protected amine designed for use as a click-chemistry reagent in PROTAC synthesis and bioconjugation. It participates in strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing partners, offering modular attachment and improved handling for linker assembly.
- Click-reactive DBCO group enables strain-promoted alkyne-azide cycloaddition (SPAAC).
- Peg3 spacer improves solubility and reduces steric hindrance.
- Fmoc-protected amine allows compatibility with solid-phase and solution-phase synthesis workflows.
- High purity suitable for research applications.
- Stable as powder at -20°C for extended storage and recommended cold storage in solution.
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Medchemexpress LLC Ms-PEG5-t-butyl ester | 870487-48-2 | MFCD20926382 | 95.0% | C16H32O9S | 10MG
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Ms-PEG5-t-butyl ester is a PEG-based linker featuring a t-butyl-protected carboxyl group, designed for use in the chemical synthesis of PROTAC molecules. It provides a hydrophilic spacer to connect ligands while masking the carboxylate during multi-step syntheses.
- Provides a hydrophilic polyethylene glycol spacer to improve solubility.
- Contains a t-butyl-protected carboxyl group for orthogonal protection during synthesis.
- Compatible with standard coupling and deprotection chemistries used in medicinal chemistry.
- Facilitates assembly of bifunctional degraders by spacing ligands and reducing steric hindrance.
- Available in small-scale quantities suitable for research and discovery workflows.
- Reported high purity suitable for synthetic applications; verify with certificate of analysis.
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Medchemexpress LLC HO-PEG3-(CH2)6-Cl | 1355955-95-1 | MFCD32705069 | 98.0% | 268.78 g/mol | C12H25ClO4 | 25 MG
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HO-PEG3-(CH2)6-Cl is a PEG3-based PROTAC linker containing a six-carbon chloroalkyl spacer and a terminal hydroxyl. It is supplied as a small-mass research chemical for use in chemical biology and targeted protein degradation research.
- PEG3 spacer with flexible ether linkages.
- Terminal hydroxyl and chloro groups for orthogonal conjugation.
- Molecular formula C12H25ClO4 and molecular weight 268.78 g/mol.
- Provided as a 25 mg research sample.
- Intended for research use; consult product documentation for storage and purity.
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Medchemexpress LLC Azido-PEG3-SSPy | 98.6% | 344.45 g·mol⁻¹ | C13H20N4O3S2 | 100 MG
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Azido-PEG3-SSPy is a cleavable three-unit polyethylene glycol (PEG3) linker used for assembling antibody-drug conjugates (ADCs) and general bioconjugation. It contains an azide functional group enabling copper-catalyzed azide-alkyne cycloaddition (CuAAC) and is compatible with strain-promoted azide-alkyne cycloaddition (SPAAC) with DBCO or BCN partners.
- Cleavable disulfide linker for controlled release.
- Azide-functionalized for CuAAC click chemistry.
- Compatible with SPAAC (DBCO and BCN) reactions.
- High purity suitable for conjugation workflows.
- Multiple pack sizes available for research use.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000369261 TCO-PEG3-NH2 50MG
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