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2-[2-[2-T-BOC-AMINOETHOXY]ETHOXY]ETHYL BROMIDE, also known as N-Boc-PEG2-bromide, is a PEG linker that features a Boc-protected amine and a bromide group. The Boc protection allows for mild acidic deprotection of the amine, while the bromide serves as an excellent leaving group for nucleophilic substitution reactions. The hydrophilic PEG spacer enhances solubility in aqueous media, making it a versatile compound for various applications.

165963-71-3

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165963-71-3 Usage

Uses

Used in Chemical Synthesis:
2-[2-[2-T-BOC-AMINOETHOXY]ETHOXY]ETHYL BROMIDE is used as a cross-linking reagent for promoting nucleophilic substitution reactions in chemical synthesis processes. The bromide group acts as a leaving group, facilitating the formation of new covalent bonds with target molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[2-[2-T-BOC-AMINOETHOXY]ETHOXY]ETHYL BROMIDE is used as a building block for the synthesis of complex drug molecules. The Boc-protected amine allows for selective deprotection and functionalization, enabling the creation of diverse pharmaceutical compounds with specific therapeutic properties.
Used in Bioconjugation:
2-[2-[2-T-BOC-AMINOETHOXY]ETHOXY]ETHYL BROMIDE is used as a bioconjugation agent for the attachment of biologically active molecules, such as peptides, proteins, or other biomolecules, to various surfaces or carriers. The PEG spacer provides hydrophilicity and stability, while the Boc-protected amine allows for selective modification of the biomolecule.
Used in Drug Delivery Systems:
In drug delivery systems, 2-[2-[2-T-BOC-AMINOETHOXY]ETHOXY]ETHYL BROMIDE is used as a component in the design of targeted drug carriers. The PEG spacer and Boc-protected amine can be utilized to attach drug molecules or targeting ligands, enhancing the solubility, bioavailability, and targeting efficiency of the drug delivery system.
Chemical Properties:
2-[2-[2-T-BOC-AMINOETHOXY]ETHOXY]ETHYL BROMIDE is a yellow oil, indicating its lipophilic nature and potential for use in various organic solvents and chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 165963-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,9,6 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 165963-71:
(8*1)+(7*6)+(6*5)+(5*9)+(4*6)+(3*3)+(2*7)+(1*1)=173
173 % 10 = 3
So 165963-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H22BrNO4/c1-11(2,3)17-10(14)13-5-7-16-9-8-15-6-4-12/h4-9H2,1-3H3,(H,13,14)

165963-71-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(2-t-Boc-aminoethoxy]ethoxy]ethyl Bromide

1.2 Other means of identification

Product number -
Other names tert-butyl N-[2-[2-(2-bromoethoxy)ethoxy]ethyl]carbamate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:165963-71-3 SDS

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