Phenylcarbamic acid esters
eMolecules 187610-67-9 | 1-BOC-AMINO-CYCLOHEXYLMETHANOL | AstaTech | MFCD04038541 | 229.320 | C12H23NO3 | 97.000 | CC(C)(C)OC(=O)NC1(CO)CCCCC1 | 5g | 448296535
1-BOC-AMINO-CYCLOHEXYLMETHANOL | AstaTech | 187610-67-9 | MFCD04038541 | 229.320 | C12H23NO3 | 97.000 | CC(C)(C)OC(=O)NC1(CO)CCCCC1 | 5g | 448296535
Medchemexpress LLC N-Desmethyl citalopram-d4 oxalate | 2747915-54-2 | C21H17D4FN2O5 | 1 MG
N-Desmethyl citalopram-d4 (oxalate) is a deuterium-labeled N-Desmethyl citalopram oxalate. It can be utilized as a tracer or internal standard for quantitative analysis using techniques such as NMR, GC-MS, or LC-MS. Stable heavy isotopes, like deuterium, are incorporated into drug molecules to aid quantitation during drug development and can influence pharmacokinetic and metabolic profiles.
- Can be used as a tracer.
- Serves as an internal standard for quantitative analysis (NMR, GC-MS, LC-MS).
- Features stable heavy isotopes for drug development quantitation.
- Potential to influence pharmacokinetic and metabolic profiles of drugs.
Medchemexpress LLC (±)-Boc-α-phosphonoglycine trimethyl ester | 89524-98-1 | 297.24 | 5 G
(±)-Boc-α-phosphonoglycine trimethyl ester is a chemical compound that functions as a glycine equivalent and glycine donor in organic synthesis. It is characterized by strong α-proton acidity, and its reaction byproducts are highly water-soluble, facilitating easy purification. This compound is effectively used to obtain 5,6- and 5,8-dimethoxy-substituted ester products through a sequence of four mild reactions.
- Serves as a glycine equivalent and glycine donor
- Exhibits strong alpha-proton acidity
- Reaction byproducts are water-soluble and easy to purify
- Efficiently obtains 5,6- and 5,8-dimethoxy-substituted ester products
- Achieves results via four mild reactions
Medchemexpress LLC 4-(4-Boc-piperazinemethyl)phenylboronic acid pinacol ester | 470478-90-1 | 98.5% | C21H33BN2O4 | 50 G
4-(4-Boc-piperazinemethyl)phenylboronic acid pinacol ester is a PROTAC linker that can be utilized in the synthesis of CST905. PROTACs consist of two distinct ligands connected by a linker, one targeting an E3 ubiquitin ligase and the other targeting the protein of interest. These compounds leverage the intracellular ubiquitin-proteasome system to facilitate the selective degradation of target proteins.
- Functions as a PROTAC linker
- Can be used in the synthesis of certain PROTAC compounds
- Designed to target E3 ubiquitin ligases and specific proteins of interest
- Utilizes the ubiquitin-proteasome system for targeted protein degradation
Medchemexpress LLC Carbamic acid, N-(6-bromohexyl)-, 1,1-dimethylethyl ester | 142356-33-0 | MFCD06201019 | 98.0% | 280.20 g/mol | C11H22BrNO2 | 25 G
Boc-NH-C6-Br is a Boc-protected 6-bromohexyl linker used as a non-cleavable linker in antibody-drug conjugate (ADC) research. It features a Boc-protected primary amine for selective deprotection and a terminal bromide for nucleophilic substitution, enabling conjugation to payloads or scaffolds.
- Provides a Boc-protected primary amine for controlled deprotection.
- Contains a terminal bromide for alkylation or substitution reactions.
- Functionally suited as a non-cleavable linker in ADC synthesis.
- Supplied with high purity for research applications.
- Available in multiple package sizes for scale flexibility.
- Data sheet, COA, and SDS available for characterization and safety information.
eMolecules 1818294-42-6 | Amino-PEG10-Boc | Ambeed | MFCD26127812 | 585.732 | C27H55NO12 | 95.000 | CC(C)(C)OC(=O)CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN | 250mg | 599120009
Amino-PEG10-Boc | Ambeed | 1818294-42-6 | MFCD26127812 | 585.732 | C27H55NO12 | 95.000 | CC(C)(C)OC(=O)CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN | 250mg | 599120009
Medchemexpress LLC Bromo-PEG2-C2-Boc | 1381861-91-1 | 97.0% | C11H21BrO4 | 250 MG
Bromo-PEG2-C2-Boc is a PEG-based PROTAC linker used in the synthesis of PROTACs. It is for research use only and exploits the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Exploits intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
Medchemexpress LLC Acid-PEG4-C2-Boc | 1835759-85-7 | 98.3% | 350.40 | 50 MG
Acid-PEG4-C2-Boc is a PEG- and Alkyl/ether-based PROTAC linker. It can be used in the synthesis of PROTACs for the inhibition of mTOR. This product is for research use only and is not sold to patients.
- PEG- and alkyl/ether-based linker
- Aids in the synthesis of PROTACs
- Assists in the inhibition of mTOR
Cambridge Isotope Laboratories NAB (N-nitrosoanabasine) (unlabeled) 0 5 mg/mL in acetonitrile 1 2 mL
NAB (N-nitrosoanabasine) (unlabeled) 0 5 mg/mL in acetonitrile 1 2 mL
Selleck Chemical LLC N-Methylsarcosine
N-Methylsarcosine (N N-Dimethylglycine (Dimethylamino)acetic acid) is a natural N-methylated glycine that is used in the development of glycine-based ionic liquids and emulsifiers
Medchemexpress LLC Mouse CD3+ T Cells Negative Selection Kit | 1 ML
The Mouse CD3+ T Cells Negative Selection Kit is designed for the isolation of CD3+ T cells from single cell suspensions of mouse spleen cells and lymph nodes. It employs a biotin-labeled monoclonal antibody to mark non-target cells, which are subsequently removed using streptavidin-labeled magnetic beads. This user-friendly, portable kit provides high-purity cells suitable for various downstream applications.
- Enables sorting of target cells in as little as 15 minutes.
- Eliminates the need for separation columns by using a magnetic separator for swift cell separation.
- Can yield sorted cells with a purity exceeding 95%.
- Sorted cells are free of antibody and magnetic bead labeling, and retain high activity and functionality for downstream experiments.
Medchemexpress LLC Boc-aminoxy-PEG4-acid | 2062663-68-5 | 98.0% | C16H31NO9 | 25 MG
Boc-aminoxy-PEG4-acid is a PEG-based PROTAC linker. It can be used in the synthesis of PROTACs, which are compounds containing two different ligands connected by a linker. One ligand is 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.
- Functions as a PEG-based PROTAC linker
- Useful in the synthesis of PROTAC compounds
- Facilitates targeted protein degradation via the ubiquitin-proteasome system
- Connects ligands for E3 ubiquitin ligase and target proteins
Medchemexpress LLC N-Boc-N-bis(C2-PEG1-azide) | 2100306-79-2 | 25 MG
N-Boc-N-bis(C2-PEG1-azide) | 2100306-79-2 | 25 MG
eMolecules 111721-74-5 | 2-Bromo-5-iodoaniline | ChemScene | MFCD16038675 | 297.921 | C6H5BrIN | 97.000 | Nc1cc(I)ccc1Br | 5g | 717420087
2-Bromo-5-iodoaniline | ChemScene | 111721-74-5 | MFCD16038675 | 297.921 | C6H5BrIN | 97.000 | Nc1cc(I)ccc1Br | 5g | 717420087
eMolecules 57260-73-8 | 1-Boc-amino-1,2-ethanediamine | Advanced ChemBlocks - In Stock | MFCD00191871 | 160.217 | C7H16N2O2 | 97.000 | CC(C)(C)OC(=O)NCCN | 5g | 416818525
1-Boc-amino-1,2-ethanediamine | Advanced ChemBlocks - In Stock | 57260-73-8 | MFCD00191871 | 160.217 | C7H16N2O2 | 97.000 | CC(C)(C)OC(=O)NCCN | 5g | 416818525