881-57-2

Basic information

• Product Name: CHEMBRDG-BB 9071542
• Synonyms: CHEMBRDG-BB 9071542;5-FORMYL-2-METHOXYPHENYL ACETATE;5-formyl-2-methoxyphenyl acetate(SALTDATA: FREE);O-Acetyl Isovanillin;3-Acetoxy-4-Methoxybenzaldehyde;3-(Acetyloxy)-4-Methoxy-benzaldehyde;3-Hydroxy-p-anisaldehyde Acetate;(5-methanoyl-2-methoxy-phenyl) ethanoate
• CAS NO: 881-57-2
• Molecular Formula: C₁₀H₁₀O₄
• Molecular Weight: 194.19
• Product Categories: Aromatics;Intermediates
• Mol File: 881-57-2.mol
• Article Data: 15

Chemical Properties

• Melting Point: 85.0 to 89.0 °C
• Boiling Point: 293°C at 760 mmHg
• Flash Point: 127.4°C
• Appearance: /
• Density: 1.193g/cm³
• Vapor Pressure: 0.00177mmHg at 25°C
• Refractive Index: 1.539
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: Dichloromethane
• CAS DataBase Reference: CHEMBRDG-BB 9071542(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 9071542(881-57-2)
• EPA Substance Registry System: CHEMBRDG-BB 9071542(881-57-2)

Safety Data

• Hazardous Substances Data: 881-57-2(Hazardous Substances Data)

Usage

Chemical Properties

Light Yellow Solid

InChI:InChI=1/C10H10O4/c1-7(12)14-10-5-8(6-11)3-4-9(10)13-2/h3-6H,1-2H3

Upstream product

• 621-59-0 isovanillin 
• 108-24-7 acetic anhydride 
• 123-08-0 4-hydroxy-benzaldehyde 
• 186581-53-3 diazomethane 
• 65298-99-9 acetic acid 5-formyl-2-hydroxy-phenyl ester 
• 113042-92-5 (E)-3,3'-diacetoxy-4'-methoxy-5-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)stilbene 
• 71155-68-5 3-Acetoxy-4-methoxy-1-(diacetoxymethyl)benzene 
• 1225192-73-3 C₁₀H₁₃NO₃ 
• 75-36-5 acetyl chloride 
• 69048-79-9 4-bromo-5-formyl-2-methoxyphenyl acetate 
• 2973-59-3 2-bromoisovanillin 

Downstream Products

• 100976-73-6 5t-(3-acetoxy-4-methoxy-phenyl)-penta-2t,4-dienoic acid methyl ester 
• 60444-56-6 3-acetoxy-4-methoxybenzoic acid 
• 81109-23-1 (3S,4R)-3-(3-Acetoxy-4-methoxy-phenyl)-8-hydroxy-1-oxo-isochroman-4-carboxylic acid 
• 134841-10-4 (2E)-3-[(3-acetyloxy)-4-methoxyphenyl]acrylic acid 
• 99179-72-3 3-acetoxy-4-methoxyphenol 
• 78515-18-1 Acetic acid 5-[(E)-2-(3-acetoxy-4-methoxy-phenyl)-vinyl]-2-methoxy-phenyl ester 
• 71198-73-7 (Z)-2-methoxy-5-((2-methyl-5-oxooxazol-4(5H)-ylidene)methyl)phenyl acetate 
• 115231-60-2 4-Methoxy-3-acetoxy-α-nitromethyl-benzylalkohol 
• 511295-05-9 5-chloro-O-acetyl isovanilline 
• 57627-75-5 5-(3-hydroxy-propyl)-2-methoxy-phenol 
• 54246-06-9 3-chloro-5-hydroxy-4-methoxybenzaldehyde 
• 511295-25-3 3-chloro-5-[1,3]dioxan-2-yl-2-methoxy-phenol 
• 511295-06-0 3-chloro-5-(1,3-dioxan-2-yl)-2-methoxyphenyl trifluoromethane sulfonate 
• 511295-24-2 5-Chloro-5'-[2-(4'-formyl-4,2'-dimethoxy-biphenyl-2-yl)-ethyl]-6,2'-dimethoxy-biphenyl-3-carbaldehyde 

Relevant articles and documents

Electrochemical detection of atrazine in wastewater samples by copper oxide (CuO) nanoparticles ionic liquid modified electrode

In the present report, a new voltammetric sensor based on copper oxide nanoparticles involved in 2-(3-acetoxy-4-methoxybenzylidenamino)-thiophenol (AMT) ionic liquid (CuO NPs/ILs) was developed for atrazine (ATR) analysis. Firstly, the CuO NPs/ILs modifie

A modified Cu(0)-Cu(I)-mediated Caryl-CarylUllmann coupling for the synthesis of biaryls

A novel Cu(0)-Cu(I)-mediated Caryl-CarylUllmann coupling has been successfully developed. The use of Cu(I) salts allowed the reactions to proceed under relatively mild conditions (65?°C in DMSO for 15–72?h). The developed method was compatible with a relatively wide range of functional groups simultaneously present on the aromatic ring of different electronic nature. The aryl halides with an electron-withdrawing group ortho to the halide or an electron-donating group meta or para to the halide furnished the corresponding products in good to excellent yields (up to 98%).

Exploring the formation and recognition of an important G-quadruplex in a HIF1α promoter and its transcriptional inhibition by a benzo[c]phenanthridine derivative

Four putative G-quadruplex sequences (PGSs) in the HIF1α promoter and the 5′UTR were evaluated for their G-quadruplex-forming potential using ESI-MS, CD, FRET, DMS footprinting, and a polymerase stop assay. An important G-quadruplex (S1) has been proven to inhibit HIF1α transcription by blocking AP2 binding. A benzo[c]phenanthridine derivative was found to target the S1 G-quadruplex and induce its conformational conversion from antiparallel to parallel orientation. The transcriptional suppression of HIF1α by this compound was demonstrated using western blotting, Q-RT-PCR, luciferase assay, and ChIP. Our new findings provided a novel strategy for HIF1α regulation and potential insight for cancer therapy.