24566-80-1

Basic information

• Product Name: N-(10-BROMODECYL)PHTHALIMIDE
• Synonyms: N-(10-BROMODECYL)PHTHALIMIDE;2-(10-BROMODECYL)ISOINDOLE-1,3-DIONE;N-(10-Bromodecyl)phthalimide, 96 %;N-(10-Bromodec-1-yl)phthalimide;2-(10-Bromodec-1-yl)-1H-isoindole-1,3(2H)-dione, 2-(10-Bromodec-1-yl)isoindolin-1,3-dione;2-(10-Bromodecyl)isoindoline-1,3-dione
• CAS NO: 24566-80-1
• Molecular Formula: C₁₈H₂₄BrNO₂
• Molecular Weight: 366.29
• Mol File: 24566-80-1.mol
• Article Data: 34

Chemical Properties

• Melting Point: 58 °C
• Boiling Point: 451.4 °C at 760 mmHg
• Flash Point: 226.8 °C
• Appearance: /
• Density: 1.283 g/cm³
• Vapor Pressure: 2.43E-08mmHg at 25°C
• Refractive Index: 1.556
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: -2.11±0.20(Predicted)
• CAS DataBase Reference: N-(10-BROMODECYL)PHTHALIMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(10-BROMODECYL)PHTHALIMIDE(24566-80-1)
• EPA Substance Registry System: N-(10-BROMODECYL)PHTHALIMIDE(24566-80-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 24566-80-1(Hazardous Substances Data)

Usage

General Description

N-(10-Bromodecyl)phthalimide is a chemical compound that falls under the class of organic compounds known as N-alkylated phthalimides. It is known for its distinctive features, which include a bromodecyl group attached to an N-atom and a phthalimide group attached to the same N-atom. Its molecular formulation is C18H22BrNO2. This particular compound has significant potential and can be used in various fields including organic synthesis, pharmaceuticals, agrochemicals, and dyestuffs. As it's mainly used as an intermediate, it has limited information regarding its toxicity. Handling and usage of such chemical compounds should always be done under controlled conditions to ensure safety.

InChI:InChI=1/C18H24BrNO2/c19-13-9-5-3-1-2-4-6-10-14-20-17(21)15-11-7-8-12-16(15)18(20)22/h7-8,11-12H,1-6,9-10,13-14H2

Upstream product

• 136918-14-4 phthalimide 
• 4101-68-2 1,10-dibromodecane 
• 1074-82-4 potassium phtalimide 

Downstream Products

• 103047-05-8 2-[10-(4-nitrophenoxy)decyl]-1H-isoindole-1,3(2H)-dione 
• 153506-41-3 2-<5-(phthalimido)decyloxy>benzaldehyde 
• 92487-43-9 2-(10-bromodecyl)-2,3-dihydro-3-hydroxy-3-phenylethynyl-1H-isoindol-1-one 
• 65325-37-3 2-[10-(Methyl-phenyl-amino)-decyl]-isoindole-1,3-dione 
• 120818-68-0 [10-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-decyl]-phosphonic acid diethyl ester 
• 866229-45-0 2-(10-{4-[tris-(4-tert-butyl-phenyl)-methyl]-phenoxy}-decyl)-isoindole-1,3-dione 
• 1036759-20-2 (2-Methoxy-5-methyl-phenyl)-carbamic acid (1R,3R,5S)-9-[10-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-decyl]-9-aza-bicyclo[3.3.1]non-3-yl ester 
• 913815-84-6 N-(9-(6-aminodecyl)-9-azabicyclo[3.3.1]nonan-3α-yl)-N'-(2-methoxy-5-methylphenyl)carbamate 
• 10496-18-1 didecyl disulfide 
• 10496-15-8 dihexyl disulfide 
• 866229-46-1 10-{4-[tris-(4-tert-butyl-phenyl)-methyl]-phenoxy}-decylamine 
• 866229-47-2 [1,3,6,8-tetraoxo-7-(10-{4-[tris-(4-tert-butyl-phenyl)-methyl]-phenoxy}-decyl)-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl]-acetic acid 
• 153506-44-6 diethyl 2,6-dimethyl-4-<2-<5-(phthalimido)decoxy>phenyl>-1,4-dihydropyridine-3,5-dicarboxylate 
• 97946-35-5 10-[4-(6,7,9,10,12,13,15,16,18,19-Decahydro-5,8,11,14,17,20-hexaoxa-benzocyclooctadecen-2-ylazo)-phenoxy]-decylamine 

Relevant articles and documents

Rotaxane-branched dendrimers with enhanced photosensitization

During the past few decades, fabrication of functional rotaxane-branched dendrimers has become one of the most attractive yet challenging topics within supramolecular chemistry and materials science. Herein, we present the successful fabrication of a fami

Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly

Despite a growing understanding of factors that drive monomer self-assembly to form supramolecular polymers, the effects of aromaticity gain have been largely ignored. Herein, we document the aromaticity gain in two different self-assembly modes of squara

Reversible diels–alder reactions with a fluorescent dye on the surface of magnetite nanoparticles

Diels–Alder reactions on the surface of nanoparticles allow a thermoreversible functionalization of the nanosized building blocks. We report the synthesis of well-defined magnetite nanoparticles by thermal decomposition reaction and their functionalizatio

Artificial Light-Harvesting Systems Based on AIEgen-branched Rotaxane Dendrimers for Efficient Photocatalysis

Aiming at the construction of novel platform for efficient light harvesting, the precise synthesis of a new family of AIEgen-branched rotaxane dendrimers was successful realized from an AIEgen-functionalized [2]rotaxane through a controllable divergent ap