118839-29-5

Basic information

• Product Name: N-(2-N,N-dihydroxyethyl)phthalimide
• Synonyms: N-(2-N,N-dihydroxyethyl)phthalimide
• CAS NO: 118839-29-5
• Molecular Formula: C₁₄H₁₈N₂O₄
• Molecular Weight: 278.306
• Mol File: 118839-29-5.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-N,N-dihydroxyethyl)phthalimide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-N,N-dihydroxyethyl)phthalimide(118839-29-5)
• EPA Substance Registry System: N-(2-N,N-dihydroxyethyl)phthalimide(118839-29-5)

Safety Data

• Hazardous Substances Data: 118839-29-5(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
N-(2-N,N-dihydroxyethyl)phthalimide serves as a valuable reagent in organic synthesis, facilitating the creation of a range of chemical products due to its unique structure and reactive functional groups.
Used as a Corrosion Inhibitor:
In industrial applications, N-(2-N,N-dihydroxyethyl)phthalimide is utilized as a corrosion inhibitor, particularly effective in preventing the corrosion of metals in acidic environments, thereby enhancing the longevity and performance of metal components.
Used in Pharmaceutical and Agrochemical Synthesis:
N-(2-N,N-dihydroxyethyl)phthalimide also acts as a precursor in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products that can improve health and crop yields.
Used in Polymer Production:
N-(2-N,N-dihydroxyethyl)phthalimide finds application in the production of polymers, where its chemical properties allow for the creation of polymers with specific characteristics required for various uses.
Used in Dye Manufacturing:
In the dye industry, this compound is employed in the manufacturing process, enabling the production of dyes with particular color and stability properties for use in textiles, printing, and other applications.
Overall, N-(2-N,N-dihydroxyethyl)phthalimide is a significant compound in the chemical industry, with a broad spectrum of applications that highlight its versatility and importance.

Upstream product

• 574-98-1 2-(2-bromoethyl)isoindoline-1,3-dione 
• 111-42-2 2,2'-iminobis[ethanol] 

Downstream Products

• 3197-06-6 N,N-bis(2-hydroxyethyl)ethylidenediamine 
• 646506-10-7 C₆₇H₈₁N₆O₁₇PSi 

Relevant articles and documents

Synthesis and properties of oligo-2′-deoxyribonucleotides containing internucleotidic phosphoramidate linkages modified with pendant groups ending with either two amino or two hydroxyl functions

Single and multiple incorporations of stereochemically pure modified dinucleoside-phosphoramidates involving substituent groups ending with bis-hydroxyethyl and bis-aminoethyl groups have been performed into pyrimidic triple helix-forming oligo-2′-deoxyribonucleotides designed to bind parallel to the purine strand of the DNA target. The ability of these modified oligo-2′-deoxyribonucleotides to form triple helices has been studied by UV-melting curve analyses, and circular dichroism. Only the oligonucleotides involving modified phosphate groups with the Rp configuration formed more stable triple helices than did the parent phosphodiester sequences. Incorporating the modifications into the third oligonucleotide strands has little effect on the structure of the triplexes. At pH 7, the incorporation of two, three or four modified phosphate groups into the third strands stabilizes the triplexes, as compared to the unmodified oligonucleotide. Stronger stabilization was observed with compounds containing linkers ending with amino functions. Stability increases with the number of modifications without being fully additive. This might be due to the different environments of the phosphate groups inside the sequence.

Substituted amine derivatives, their production and use

Substituted amino derivatives represented by the formula: STR1 wherein R1 and R2 each stand for an acyclic hydrocarbon residue or an alicyclic hydrocarbon residue; R3 and R4 each stand for hydrogen or a hydrocarbon residue optionally containing hetero-atom(s); A stands for a carbon chain having two or more carbon atoms optionally containing ether linkage or sulfide linkage, which may be substituted and which may per se form a ring; X1 and X2 each stand for oxygen atom or sulfur atom; and Y stands for amino group or an organic residue bonded through nitrogen atom, which may form a ring by combining with a carbon atom constituting A; and their salts have anti-arrhythmic activity and are useful for prevention and treatment of a variety of arrhythmias.