CAS Number57671-28-0
Synonyms1-Phenyl-2,5,8,11,14-pentaoxahexadecan-16-ol; 2-[2-[2-[2-(2-phenylmethoxyethoxy)ethoxy]ethoxy]ethoxy]ethanol
Molecular FormulaC17H28O6
Molecular Weight328.41
Purity98.00%
Density1.1±0.1 g/cm3
Boiling Point437.2±40.0 °C at 760 mmHg
AppearanceVery light yellow - yellow transparent liquid
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 57671-28-0 |
| Catalog No. | 2A-9044880 |
| Chinese Name | 五甘醇单苄基醚 |
| Synonyms | 1-Phenyl-2,5,8,11,14-pentaoxahexadecan-16-ol; 2-[2-[2-[2-(2-phenylmethoxyethoxy)ethoxy]ethoxy]ethoxy]ethanol |
| Molecular Formula | C17H28O6 |
| Molecular Weight | 328.41 |
| Purity | 98.00 |
| Density | 1.1±0.1 g/cm3 |
| Boiling Point | 437.2±40.0 °C at 760 mmHg |
| Appearance | Very light yellow - yellow transparent liquid |
| Storage Condition | Keep the container sealed and stored in a cool, dr |
| Application | BnO-PEG5-OH is a PEG-based PROTAC linker that can be used for PROTAC synthesis. |
| HTC | 2909499000 |
| MDL Number | MFCD06797154 |
| SMILES | OCCOCCOCCOCCOCCOCc1ccccc1 |
| InChI Key | UMUSOTNGYAALST-UHFFFAOYSA-N |
| MSDS | msds/44880_1_57671_28_0.pdf |
| Bioactivity | BnO-PEG5-OH is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Related Catalog Research Areas >> Cancer Signaling Pathways >> PROTAC >> PROTAC Linker Target PEGs In Vitro 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. References [1]. Girardini M, et al. Cereblon versus VHL: Hijacking E3 ligases against each other using PROTACs. Bioorg Med Chem. 2019 Jun 15;27(12):2466-2479. Chemical & Physical Properties Density 1.1±0.1 g/cm3 Boiling Point 437.2±40.0 °C at 760 mmHg Molecular Formula C17H28O6 Molecular Weight 328.401 Flash Point 218.2±27.3 °C Exact Mass 328.188599 PSA 66.38000 LogP -0.18 Vapour Pressure 0.0±1.1 mmHg at 25°C Index of Refraction 1.497 InChIKey UMUSOTNGYAALST-UHFFFAOYSA-N SMILES OCCOCCOCCOCCOCCOCc1ccccc1 |
| Use of | BnO-PEG5-OH is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Properties Name Pentaethylene Glycol Monobenzyl Ether Synonym More Synonyms BnO-PEG5-OH Biological Activity Description BnO-PEG5-OH is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Related Catalog Research Areas >> Cancer Signaling Pathways >> PROTAC >> PROTAC Linker In Vitro 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. References Chemical & Physical Properties Molecular Formula C17H28O6 Exact Mass 328.188599 PSA 66.38000 LogP -0.18 Index of Refraction 1.497 InChIKey UMUSOTNGYAALST-UHFFFAOYSA-N |
| Tax Rebate | 9.0% |
| Supervision | None MFN tariff: 5.5% Ordinary tariff: 30.0% |
| Transport Info | Product name: Purity: 97.0% |
| MSDS Transport Info | Module 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified |
| Related Products in Specialty Chemicals | ||
|---|---|---|
| 1,3-Propanediol bis(4-aminobenzoate) | 57609-64-0 | 2A-9044873 |
| 4-[2-[5-[4-(Diethylamino)phenyl]-4,5-dihydro-1-phenyl-1H-pyrazol-3-yl]vinyl]-N,N-diethylaniline | 57609-72-0 | 2A-9044874 |
| Methyl 2,2-dimethylphenylacetate | 57625-74-8 | 2A-9044876 |
| Timiperone | 57648-21-2 | 2A-9044877 |
| 3-(3-Methyl-1H-indol-1-yl)propanoic acid | 57662-47-2 | 2A-9044879 |
| 2-Carbomethoxybenzenesulfonamide | 57683-71-3 | 2A-9044882 |
| Acid Black 172 | 57693-14-8 | 2A-9044883 |
| 1'-Hydroxybufuralol | 57704-16-2 | 2A-9044886 |
| 2,4,6-Tribromothiophenol | 57730-98-0 | 2A-9044889 |
| 4-Acetyl-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine | 57756-36-2 | 2A-9044892 |
| Browse all Specialty Chemicals products » | ||
Phone:
630-322-8886
630-322-8887
Email:
Office Locations:
Chicago, IL, USA
San Francisco, CA, USA
EN
SDS