t-boc-N-amido-PEG7-alcohol
N-Boc-PEG7-alcohol
CAS: 1292268-13-3
Molecular Formula: C19H39NO9
t-boc-N-amido-PEG7-alcohol - Names and Identifiers
t-boc-N-amido-PEG7-alcohol - Physico-chemical Properties
| Molecular Formula | C19H39NO9 |
| Molar Mass | 425.51 |
| Density | 1.090±0.06 g/cm3(Predicted) |
| Boling Point | 521.1±50.0 °C(Predicted) |
| pKa | 12.23±0.46(Predicted) |
| Storage Condition | 室温，干燥，密封 |
| MDL | MFCD29049415 |
| In vitro study | 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. ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker. |
t-boc-N-amido-PEG7-alcohol - Introduction
N-Boc-PEG7-alcohol is a hydrophobic polyethylene glycol derivative. Its chemical structure contains a protecting group (Boc Group) and seven PEG (polyethylene glycol) units.
N-Boc-PEG7-alcohol has good solubility and stability, and can be widely used in pharmaceutical chemistry, biochemistry, materials science and other fields. One of the most common applications is as a synthetic intermediate for drug molecules. It can be used as an esterification reagent or activator for the synthesis of pharmaceutically active molecules.
The preparation method of N-Boc-PEG7-alcohol usually adopts synthetic chemical method. The specific method includes first reacting the N-Boc-PEG7 diamine with a suitable alcohol, and then removing the protecting group Boc through a series of reaction steps to finally obtain the N-Boc-PEG7-alcohol product.
It is necessary to pay attention to its safety when handling N-Boc-PEG7-alcohol. It may be irritating to the skin, eyes and respiratory system and may be harmful to the environment. Appropriate protective measures should be taken during use, including wearing protective gloves, goggles and protective masks. In addition, it should be used in a well-ventilated place and avoid contact with oxidants and high temperatures to prevent the production of hazardous substances or fire.
N-Boc-PEG7-alcohol has good solubility and stability, and can be widely used in pharmaceutical chemistry, biochemistry, materials science and other fields. One of the most common applications is as a synthetic intermediate for drug molecules. It can be used as an esterification reagent or activator for the synthesis of pharmaceutically active molecules.
The preparation method of N-Boc-PEG7-alcohol usually adopts synthetic chemical method. The specific method includes first reacting the N-Boc-PEG7 diamine with a suitable alcohol, and then removing the protecting group Boc through a series of reaction steps to finally obtain the N-Boc-PEG7-alcohol product.
It is necessary to pay attention to its safety when handling N-Boc-PEG7-alcohol. It may be irritating to the skin, eyes and respiratory system and may be harmful to the environment. Appropriate protective measures should be taken during use, including wearing protective gloves, goggles and protective masks. In addition, it should be used in a well-ventilated place and avoid contact with oxidants and high temperatures to prevent the production of hazardous substances or fire.
Last Update：2024-04-09 20:52:54
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Product Name: N-Boc-PEG7-alcohol Visit Supplier Webpage Request for quotationCAS: 1292268-13-3
Tel: 609-228-6898
Email: sales@medchemexpress.com
tech@medchemexpress.com
Mobile: 609-228-6898
Spot supply
Product Name: BocNH-PEG7-OH Visit Supplier Webpage Request for quotationCAS: 1292268-13-3
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
Wechat: 18621343501
WhatsApp: +86-18621343501
Spot supply
Product Name: N-Boc-PEG7-alcohol Visit Supplier Webpage Request for quotationCAS: 1292268-13-3
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328
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View History
t-boc-N-amido-PEG7-alcohol
Camphor Impurity 13
4-(azepan-1-ylmethyl)-5-hydroxy-2-methyl-N-(4-methylphenyl)-1-benzofuran-3-carboxamide
3622-91-1
Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone, 5-bromo-2,9-bis(1-propylbutyl)-
isopropyl 2-[(1-adamantylcarbonyl)amino]-4,5-dimethyl-3-thiophenecarboxylate
1-(pyridin-4-ylmethyl)-4-piperidinecarboxylic acid
Diphenylpicrylhydrazyl free radical
N-[4-(allyloxy)-3-methoxybenzyl]-N-(1H-1,2,4-triazol-3-yl)amine
3,4-Difluoro-N-(4-fluorobenzyl)benzenesulfonamide
Camphor Impurity 13
4-(azepan-1-ylmethyl)-5-hydroxy-2-methyl-N-(4-methylphenyl)-1-benzofuran-3-carboxamide
3622-91-1
Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone, 5-bromo-2,9-bis(1-propylbutyl)-
isopropyl 2-[(1-adamantylcarbonyl)amino]-4,5-dimethyl-3-thiophenecarboxylate
1-(pyridin-4-ylmethyl)-4-piperidinecarboxylic acid
Diphenylpicrylhydrazyl free radical
N-[4-(allyloxy)-3-methoxybenzyl]-N-(1H-1,2,4-triazol-3-yl)amine
3,4-Difluoro-N-(4-fluorobenzyl)benzenesulfonamide