Phenylcarbamic acid esters
Medchemexpress LLC N-Methylhydantoin | 616-04-6 | 99.9% | 114.10 | 10 G
N-Methylhydantoin is a product of degradation of creatinine by bacteria. It is classified as a Human Endogenous Metabolite and Microbial Metabolite. It is for research use only.
- Endogenous metabolite
- Microbial metabolite
- For research use only
Medchemexpress LLC 4-(4-Boc-piperazinemethyl)phenylboronic acid pinacol ester | 470478-90-1 | 98.5% | C21H33BN2O4 | 100 G
4-(4-Boc-piperazinemethyl)phenylboronic acid pinacol ester is a PROTAC linker utilized in the synthesis of CST905. This compound functions as part of Proteolysis Targeting Chimeras (PROTACs), which are molecules designed to selectively degrade target proteins by harnessing the intracellular ubiquitin-proteasome system. PROTACs achieve this by using two ligands connected by a linker: one binds to an E3 ubiquitin ligase, and the other targets a specific protein. This product is for research use only.
- Functions as a PROTAC linker
- Used in the synthesis of CST905
- Exploits the intracellular ubiquitin-proteasome system
- Designed for selective degradation of target proteins
- Purity is 98.50%
- Molecular weight is 388.31
- Appearance is solid, white to light yellow
Cayman Chemical N ketocaproylLHomoserine lac
A bacterial quorum-sensing signaling molecule; produced in the marine bioluminescence bacterium V. fischeri
eMolecules 13734-36-6 | Boc-sarcosine | Chem-Impex | MFCD00037795 | 189.211 | C8H15NO4 | 98.000 | CN(CC(O)=O)C(=O)OC(C)(C)C | 100g | 112441432
Boc-sarcosine | Chem-Impex | 13734-36-6 | MFCD00037795 | 189.211 | C8H15NO4 | 98.000 | CN(CC(O)=O)C(=O)OC(C)(C)C | 100g | 112441432
Medchemexpress LLC 3-Oxazolidinecarboxylic acid, 4-formyl-2,2-dimethyl-, 1,1-dimethylethyl ester, (4s)- | 102308-32-7 | 98.6% | C11H19NO4 | 10 G
(S)-(-)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde is a chiral compound commonly used as a chiral intermediate in asymmetric synthesis and has important applications in organic synthesis. It is a polar aldehyde substrate that can enhance the polarity, solubility, and the possibility of forming hydrogen bonds of compounds.
- It is a chiral compound.
- It is used as a chiral intermediate in asymmetric synthesis.
- It has important applications in the field of organic synthesis.
- Enhances polarity, solubility, and hydrogen bond formation.
eMolecules 288154-18-7 | 1-Boc-4-amino-4-(aminocarbonyl)piperidine | Acrotein ChemBio Inc. | MFCD04114477 | 243.307 | C11H21N3O3 | 97.000 | CC(C)(C)OC(=O)N1CCC(N)(CC1)C(N)=O | 25g | 625591641
1-Boc-4-amino-4-(aminocarbonyl)piperidine | Acrotein ChemBio Inc. | 288154-18-7 | MFCD04114477 | 243.307 | C11H21N3O3 | 97.000 | CC(C)(C)OC(=O)N1CCC(N)(CC1)C(N)=O | 25g | 625591641
![eMolecules 53292-89-0 | trans-4-(Boc-amino)cyclohexanecarboxylic acid | Combi-Blocks | MFCD01862293 | 243.303 | C12H21NO4 | 98.000 | CC(C)(C)OC(=O)N[C@H]1CC[C@@H](CC1)C(O)=O | 25g | 249365663](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000163031.jpg-250.jpg)
eMolecules 53292-89-0 | trans-4-(Boc-amino)cyclohexanecarboxylic acid | Combi-Blocks | MFCD01862293 | 243.303 | C12H21NO4 | 98.000 | CC(C)(C)OC(=O)N[C@H]1CC[C@@H](CC1)C(O)=O | 25g | 249365663
trans-4-(Boc-amino)cyclohexanecarboxylic acid | Combi-Blocks | 53292-89-0 | MFCD01862293 | 243.303 | C12H21NO4 | 98.000 | CC(C)(C)OC(=O)N[C@H]1CC[C@@H](CC1)C(O)=O | 25g | 249365663