41313-77-3

Basic information

• Product Name: 4-(BIS(2-(ACETYLOXY)ETHYL)AMINO)BENZ-
• Synonyms: 4-[Bis[2-(acetyloxy)ethyl]amino]benzaldehyde 98%;4-(BIS(2-(ACETYLOXY)ETHYL)AMINO)BENZ-
• CAS NO: 41313-77-3
• Molecular Formula: C₁₅H₁₉NO₅
• Molecular Weight: 293.317
• Product Categories: C13-C60;Carbonyl Compounds;Chemical Synthesis;Materials Science;NLO Chromophores and Intermediates;Non-Linear Optical (NLO) Materials;Organic and Printed Electronics;Organic Building Blocks;Photonic and Optical Materials;C10 to C21Photonic and Optical Materials;Aldehydes;Carbonyl Compounds;NLO Chromophores and Intermediates;Non-Linear Optical (NLO) Materials;Building Blocks
• Mol File: 41313-77-3.mol
• Article Data: 14

Chemical Properties

• Melting Point: 60-63 °C(lit.)
• Boiling Point: 193-195 °C0.08 mm Hg(lit.)
• Flash Point: 212.5 °C
• Appearance: /
• Density: 1.1687 (rough estimate)
• Vapor Pressure: 1.59E-07mmHg at 25°C
• Refractive Index: 1.5080 (estimate)
• CAS DataBase Reference: 4-(BIS(2-(ACETYLOXY)ETHYL)AMINO)BENZ-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(BIS(2-(ACETYLOXY)ETHYL)AMINO)BENZ-(41313-77-3)
• EPA Substance Registry System: 4-(BIS(2-(ACETYLOXY)ETHYL)AMINO)BENZ-(41313-77-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 41313-77-3(Hazardous Substances Data)

Usage

General Description

4-(bis(2-(acetyloxy)ethyl)amino)benz- is a chemical compound that belongs to the class of benzene derivatives. It contains a benzene ring with an amino group attached to it, as well as two acetyloxyethyl groups. 4-(BIS(2-(ACETYLOXY)ETHYL)AMINO)BENZ- is often used as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It can also be utilized as a reagent in chemical reactions due to its ability to donate or accept electrons. Additionally, it may have potential applications in medicinal chemistry and drug development due to its structural properties and functional groups.

InChI:InChI=1/C15H19NO5/c1-12(18)20-9-7-16(8-10-21-13(2)19)15-5-3-14(11-17)4-6-15/h3-6,11H,7-10H2,1-2H3

Upstream product

• 19249-34-4 bis(2-acetoxyethyl)aniline 
• 68-12-2 N,N-dimethyl-formamide 
• 108-24-7 acetic anhydride 
• 27913-86-6 4-(bis(2-hydroxyethyl)amino)benzaldehyde 
• 120-07-0 2,2'-(phenylimino)bis[ethanol] 
• 75-36-5 acetyl chloride 
• 62-53-3 aniline 

Downstream Products

• 1014690-21-1 C₃₃H₂₉NO₁₀ 
• 1248703-62-9 3,4-bis(hexyloxy)-2-{4-[N,N-di[2-(acetyloxy)ethyl]amino]styryl}thiophene 
• 1338598-46-1 C₂₉H₂₅N₃O₆ 
• 1385820-69-8 C₄₃H₄₉N₅O₆ 
• 1260401-27-1 (E)-2,2'-(4-(2-(3-dicyanomethylene)-5,5-dimethylcyclohex-1-enyl)(vinyl)phenylazanediyl)bis(ethane)bis(ethane-2,1-diyl) diacetate 
• 1315270-42-8 C₁₀H₇O₃S^(1-)*C₁₉H₂₅N₂O₃⁽¹⁺⁾ 
• 1315270-41-7 C₁₀H₇O₃S^(1-)*C₁₉H₂₅N₂O₃⁽¹⁺⁾ 
• 1315270-40-6 C₆H₅O₃S^(1-)*C₁₉H₂₅N₂O₃⁽¹⁺⁾ 
• 1315270-39-3 C₈H₉O₃S^(1-)*C₁₉H₂₅N₂O₃⁽¹⁺⁾ 
• 1315270-38-2 C₆H₆NO₃S^(1-)*C₁₉H₂₅N₂O₃⁽¹⁺⁾ 
• 1315270-37-1 C₆H₆NO₃S^(1-)*C₁₉H₂₅N₂O₃⁽¹⁺⁾ 
• 1315270-36-0 C₆H₄NO₅S^(1-)*C₁₉H₂₅N₂O₃⁽¹⁺⁾ 
• 1315270-35-9 C₆H₄NO₅S^(1-)*C₁₉H₂₅N₂O₃⁽¹⁺⁾ 
• 1315270-34-8 C₆H₄ClO₃S^(1-)*C₁₉H₂₅N₂O₃⁽¹⁺⁾ 

Relevant articles and documents

New BODIPY derivatives as OFF-ON fluorescent chemosensor and fluorescent chemodosimeter for Cu2+: Cooperative selectivity enhancement toward Cu2+

New 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) derivatives (1 and 2) were synthesized as an "off-on" fluorescent chemosensor and fluorescent chemodosimeter for Cu2+ and Pb2+. Compound 1 displayed selective and large chelation enhanced fluorescence effects with Pb2+ and Cu2+ among the metal ions examined. On the other hand, compound 2, a fluorescent chemodosimeter, effectively recognized Cu 2+ via a selective hydrolysis of the acetyl group.

Double-cyano stilbene ethylene two-photon fluorescent solvent chromophore water-soluble probe and its synthetic method and application (by machine translation)

The invention belongs to the technical field of fine chemicals, in particular to double-cyano stilbene ethylene two-photon fluorescent solvent chromophore water-soluble probe and its synthetic method and application, the probe in order to double-cyano stilbene (DCS) for the two-photon fluorescent matrix preparation. The probe molecules of small size, good solubility in water and is suitable for solvent polarity detection, in addition to the fluorescence intensity of the probe, two-photon absorption cross section of the insured with viscosity changes obviously, display a very wide range of solvent chromophore, large two-photon absorption cross section and ultra-large Stokes displacement, thereby greatly improving the detection sensitivity, imaging resolution, sensitivity and transverse and longitudinal resolution, and the accuracy of the test; cell microscopic imaging experiment to demonstrate that its in a cell or tissue has good color range and absorption effect, can be very good detection and reflect cell change in viscosity of the situation, and itself not toxic to the cells. In biological, in the medical field has great application value. (by machine translation)

Water/alcohol soluble electron injection material containing azacrown ether groups: Synthesis, characterization and application to enhancement of electroluminescence

Using an environmentally stable metal as the cathode in a polymer light-emitting diode (PLED) is an essential requirement for its practical application. We present the preparation of a water/alcohol soluble copoly(p-phenylene) (P1) containing pendant azacrown ether and ethylene glycol ether groups as a highly efficient electron injection layer (EIL) for PLEDs, allowing the use of environmentally stable aluminum as the cathode. Multilayer PLEDs [ITO/PEDOT:PSS/PF-Green-B/EIL/Al] using P1 as EIL exhibit significantly enhanced device performance, particularly in the presence of K 2CO3 or Cs2CO3. The maximum luminous power efficiency and maximum luminance of the device with Cs2CO 3-doped P1 as EIL were enhanced to 9.16 lm W-1 and 17050 cd m-2, respectively, compared with those without EIL (0.16 lm W -1, 890 cd m-2). The turn-on voltage was also significantly reduced from 5.7 V to 3.7 V simultaneously. The performance enhancement has been attributed to improved electron injection which has been confirmed by the rise in open-circuit voltage (Voc) obtained from photovoltaic measurements. The incorporation of such an electron injection layer significantly enhances device performance for PLEDs with an environmentally stable metal as the cathode.