CAS 5181-35-1

2-(2-Bromoethoxy)-1H-isoindole-1,3(2H)-dione

Description:

2-(2-Bromoethoxy)-1H-isoindole-1,3(2H)-dione, with the CAS number 5181-35-1, is a chemical compound that features a unique structure combining an isoindole core with a bromoethoxy substituent. This compound is characterized by its heterocyclic structure, which includes a five-membered ring containing nitrogen and a carbonyl group, contributing to its reactivity and potential biological activity. The presence of the bromoethoxy group enhances its solubility in organic solvents and may influence its interaction with biological targets. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, particularly in the development of new therapeutic agents. The compound may exhibit various properties such as moderate stability under standard conditions, and its reactivity can be influenced by the presence of the bromine atom, which can participate in nucleophilic substitution reactions. Overall, 2-(2-Bromoethoxy)-1H-isoindole-1,3(2H)-dione represents a class of compounds that are of interest in medicinal chemistry and materials science.

Formula: C₁₀H₈BrNO₃

InChI: InChI=1S/C10H8BrNO3/c11-5-6-15-12-9(13)7-3-1-2-4-8(7)10(12)14/h1-4H,5-6H2

InChI key: InChIKey=OCWDBKQNNKCYCJ-UHFFFAOYSA-N

SMILES: O=C1C=2C(C(=O)N1OCCBr)=CC=CC2

Synonyms:

• 1H-isoindole-1,3(2H)-dione, 2-(2-bromoethoxy)-
• 2-(2-Bromoethoxy)-2,3-dihydro-1H-isoindole-1,3-dione
• 2-(2-Bromoethoxy)isoindole-1,3-dione
• N-(2-Bromoethoxy)phthalimide
• Phthalimide, N-(2-bromoethoxy)-
• 2-(2-Bromoethoxy)-1H-isoindole-1,3(2H)-dione
• 2-(2-Bromoethoxy)-1H-isoindole-1,3(2H)-dione

2-(2-Bromoethoxy)isoindoline-1,3-dione

CAS: 5181-35-1

Formula: C₁₀H₈BrNO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 270.0794

Ref: IN-DA003S8S

2-(2-Bromoethoxy)isoindoline-1,3-dione

CAS: 5181-35-1

2-(2-Bromoethoxy)isoindoline-1,3-dione

Purity: 95%

Molecular weight: 270.08g/mol

Ref: 54-OR1053764

2-(2-Bromoethoxy)isoindoline-1,3-dione

CAS: 5181-35-1

Formula: C₁₀H₈BrNO₃

Purity: 95%

Molecular weight: 270.082

Ref: 10-F544385

N-(2-Bromoethoxy)phthalimide

Controlled Product

CAS: 5181-35-1

Applications Reagent used in Phthalimidooxy alylation.
References Yoda, R., et al.: Chem. Pharm. Bull., 42, 686 (1994), Kim, M., et al.: Bioorg. Med. Chem. Lett., 6, 2077 (1996),

Formula: C₁₀H₈BrNO₃

Color and Shape: Neat

Molecular weight: 270.08

Ref: TR-B684215

N-(2-Bromoethoxy)phthalimide

CAS: 5181-35-1

N-(2-Bromoethoxy)phthalimide is a chemical compound that has been shown to inhibit the activity of histone deacetylases. Histones are proteins that regulate gene expression and play an important role in the regulation of DNA transcription. The enzyme histone deacetylase (HDAC) removes acetyl groups from these proteins, which can lead to changes in gene expression and misregulation of cellular processes. HDACs have been linked to autoimmune diseases, such as arthritis and multiple sclerosis, because they can cause inflammation by affecting the production of inflammatory cytokines. N-(2-Bromoethoxy)phthalimide is able to inhibit HDACs by forming covalent bonds with the lysine residues on these enzymes. This inhibition causes modifications that affect the interaction between HDACs and their substrates, preventing them from modifying histones or interacting with other proteins.

Formula: C₁₀H₈BrNO₃

Purity: Min. 95%

Molecular weight: 270.08 g/mol

Ref: 3D-FB19226