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2 3 4-(Trimethoxy)bromobenzene 99

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2 3 4-(Trimethoxy)bromobenzene 99 manufacturers

2 3 4-(Trimethoxy)bromobenzene 99 Basic information
Product Name:2 3 4-(Trimethoxy)bromobenzene 99
Synonyms:Benzene,1-bromo-2,3,4-trimethoxy-;1-Bromo-2,3,4-trimethoxybenzene;2 3 4-(Trimethoxy)bromobenzene 99
CAS:10385-36-1
MF:C9H11BrO3
MW:247.09
EINECS:
Product Categories:Ethers;Organic Building Blocks;Oxygen Compounds
Mol File:10385-36-1.mol
2 3 4-(Trimethoxy)bromobenzene 99 Structure
2 3 4-(Trimethoxy)bromobenzene 99 Chemical Properties
Boiling point 105-110 °C/2 mmHg (lit.)
density 1.291 g/mL at 25 °C (lit.)
refractive index n20/D 1.549(lit.)
Fp >230 °F
storage temp. 2-8°C
AppearanceLight yellow to yellow Liquid
InChI1S/C9H11BrO3/c1-11-7-5-4-6(10)8(12-2)9(7)13-3/h4-5H,1-3H3
InChIKeyHKCQJLVIFMFOTG-UHFFFAOYSA-N
SMILESCOc1ccc(Br)c(OC)c1OC
Safety Information
WGK Germany 3
Storage Class10 - Combustible liquids
MSDS Information
2 3 4-(Trimethoxy)bromobenzene 99 Usage And Synthesis
Uses2,3,4-(Trimethoxy)bromobenzene can be prepared from 1,2,3-(trimethoxy)benzene via bromination.
General Description2,3,4-(Trimethoxy)bromobenzene can be prepared from 1,2,3-(trimethoxy)benzene via bromination.
Synthesis
1,2,3-Trimethoxybenzene

634-36-6

2 3 4-(TRIMETHOXY)BROMOBENZENE  99

10385-36-1

General procedure for the synthesis of 2,3,4-tris(methoxy)bromobenzene from 1,2,3-trimethoxybenzene: In a dry 45 mL reaction tube equipped with a magnetic stirrer (note: the air inside the reaction tube is not displaced), 1 mL of [Bmim]NO3 as solvent, 0.5 mmol of 1,2,3-trimethoxybenzene, and 0.25 mmol of Br2 were added. The reaction tube was then sealed and the reaction was stirred at 80 °C for 24 hours. Upon completion of the reaction, the mixture was cooled to room temperature and diluted with 3 mL of water. The reaction mixture was extracted with dichloromethane (3 x 10 mL) to isolate the target product 2,3,4-tris(methoxy)bromobenzene. The GC yield of the product was determined by gas chromatography (GC) analysis. In another parallel experiment, the product was purified by column chromatography and structurally characterized using 1H NMR and 13C NMR.

References[1] Synthetic Communications, 2007, vol. 37, # 2, p. 323 - 328
[2] Australian Journal of Chemistry, 1992, vol. 45, # 12, p. 1967 - 1982
[3] Journal of Chemical Research - Part S, 1998, # 10, p. 662 - 663
[4] Russian Journal of Organic Chemistry, 2007, vol. 43, # 9, p. 1282 - 1284
[5] Synthetic Communications, 2005, vol. 35, # 14, p. 1947 - 1952
2 3 4-(Trimethoxy)bromobenzene 99 Preparation Products And Raw materials
Raw materials1,2,3-Trimethoxybenzene
Tag:2 3 4-(Trimethoxy)bromobenzene 99(10385-36-1) Related Product Information
2 3 4-(Trimethoxy)bromobenzene 99 AURORA 7596 AURORA 5734 AURORA 8292 AURORA 5315 AURORA 8249 AURORA 5350 AURORA 4592 AURORA 8149 AURORA 23145 AURORA 4601 AURORA 5246 AURORA 6715 AURORA 2022 AURORA 4591 AURORA 7667 AURORA 4593 AURORA 5245