CAS 165963-71-3

tert-butyl {2-[2-(2-bromoethoxy)ethoxy]ethyl}carbamate

Description:

Tert-butyl {2-[2-(2-bromoethoxy)ethoxy]ethyl}carbamate, identified by its CAS number 165963-71-3, is a chemical compound characterized by its carbamate functional group, which is linked to a tert-butyl group and a branched ethoxy chain containing a bromo substituent. This compound typically exhibits properties associated with carbamates, such as moderate solubility in organic solvents and potential reactivity due to the presence of the bromo group, which can participate in nucleophilic substitution reactions. The ethoxy chains contribute to its hydrophobic characteristics, while the bromoethoxy moiety may enhance its reactivity and potential applications in organic synthesis or medicinal chemistry. Additionally, the tert-butyl group provides steric hindrance, which can influence the compound's reactivity and stability. Overall, this compound may be of interest in various fields, including pharmaceuticals and agrochemicals, due to its unique structural features and potential for further functionalization.

Formula: C₁₁H₂₂BrNO₄

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)

InChI key: WGWDCMKAMHBDPO-UHFFFAOYSA-N

SMILES: CC(C)(C)OC(=NCCOCCOCCBr)O

N-Boc-PEG2-bromide

CAS: 165963-71-3

N-Boc-PEG2-bromide

Formula: C₁₁H₂₂BrNO₄

Purity: 98%

Molecular weight: 312.20067

Ref: 54-BIPG1665

tert-Butyl (2-(2-(2-bromoethoxy)ethoxy)ethyl)carbamate

CAS: 165963-71-3

Formula: C₁₁H₂₂BrNO₄

Purity: 97%

Color and Shape: Liquid

Molecular weight: 312.2007

Ref: IN-DA001WFR

N-Boc-PEG3-bromide

CAS: 165963-71-3

N-Boc-PEG3-bromide is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

Formula: C₁₁H₂₂BrNO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 312.201

Ref: TM-T16212

N-Boc-PEG2-bromide

CAS: 165963-71-3

tert-Butyl (2-(2-(2-bromoethoxy)ethoxy)ethyl)carbamate

Formula: C₁₁H₂₂BrNO₄

Purity: 97%

Molecular weight: 312.2

Ref: IN-DG291859

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

Controlled Product

CAS: 165963-71-3

Stability Light Sensitive, Moisture Sensitive
Applications A cross-linking reagent.
References Hatanaka, Y., et al.: Bioorg. Med. Chem., 2, 1367 (1994), Li, X., et al.: J. Med. Chem., 51, 3057 (2008),

Formula: C₁₁H₂₂BrNO₄

Color and Shape: Neat

Molecular weight: 312.2007

Ref: TR-B618590

tert-Butyl (2-(2-(2-bromoethoxy)ethoxy)ethyl)carbamate

CAS: 165963-71-3

Formula: C₁₁H₂₂BrNO₄

Purity: 95%

Color and Shape: Liquid

Molecular weight: 312.204

Ref: 10-F463694