N3-PEG7-OH CAS 1274892-60-2

Introduction:Basic information about N3-PEG7-OH CAS 1274892-60-2, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

N3-PEG7-OH Basic information

Product Name:N3-PEG7-OH
Synonyms:N3-PEG7-OH;Azido-PEG7-OH;20-azido-3,6,9,12,15,18-hexaoxaicosan-1-ol;N3-PEG7-OH/3,6,9,12,15,18-Hexaoxaeicosan-1-ol, 20-azido-;N?-PEG7-OH
CAS:1274892-60-2
MF:C14H29N3O7
MW:351.4
EINECS:
Product Categories:peg
Mol File:1274892-60-2.mol

N3-PEG7-OH Chemical Properties

storage temp. Store at Room Tem.
solubility Soluble in Water, DMSO, DCM, DMF
InChIInChI=1S/C14H29N3O7/c15-17-16-1-3-19-5-7-21-9-11-23-13-14-24-12-10-22-8-6-20-4-2-18/h18H,1-14H2
InChIKeyIKLKCSJOBKMTTI-UHFFFAOYSA-N
SMILESC(COCCOCCOCCO)OCCOCCOCCN=[N+]=[N-]

Safety Information

N3-PEG7-OH Usage And Synthesis

DescriptionAzido-PEG7-alcohol is a aqueous soluble PEGylation reagent The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. Hydroxy group further increase the reagnt's water solubility.
UsesAzido-PEG7-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Azido-PEG7-alcohol is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
IC 50PEGs
References[1] An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562 DOI:10.1016/j.ebiom.2018.09.005

N3-PEG7-OH Preparation Products And Raw materials

N3 CAS 2640657-07-2
N4,N4,N4',N4'-tetra([1,1'-biphenyl]-4-yl)-[1,1'-biphenyl]-4,4'-diamine CAS
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