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6-Bromoveratraldehyde

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Products Intro: Product Name:2-Bromo-4,5-dimethoxybenzaldehyde;6-Bromoveratraldehyde
CAS:5392-10-9
Purity:0.98
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CAS:5392-10-9
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CAS:5392-10-9
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6-Bromoveratraldehyde manufacturers

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  • CAS:5392-10-9
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  • Purity: 99%
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  • CAS:5392-10-9
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6-Bromoveratraldehyde Basic information
Product Name:6-Bromoveratraldehyde
Synonyms:AKOS B005109;6-BROMOVERATRALDEHYDE;TIMTEC-BB SBB003186;6-BROMOVERATRALDEHYDE 98%;2-BROMO-4,5-DIMETHOXYBENZALEHYDE;6-BROMOVEZATALDEHYDE;2-BROMO-4,5-DIMETHOXYBENZALDEHYDE / 6-BROMOVERATRALDEHYDE;4,5-Dimethoxy-2-bromobenzaldehyde
CAS:5392-10-9
MF:C9H9BrO3
MW:245.07
EINECS:226-390-4
Product Categories:Benzaldehyde;Aldehydes;C9;Carbonyl Compounds;Aromatic Aldehydes & Derivatives (substituted)
Mol File:5392-10-9.mol
6-Bromoveratraldehyde Structure
6-Bromoveratraldehyde Chemical Properties
Melting point 150-151 °C (lit.)
Boiling point 316.1±37.0 °C(Predicted)
density 1.5955 (rough estimate)
refractive index 1.4730 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to crystal
color White to Yellow to Orange
Water Solubility Insoluble in water.
Sensitive Air Sensitive
BRN 2052355
InChIInChI=1S/C9H9BrO3/c1-12-8-3-6(5-11)7(10)4-9(8)13-2/h3-5H,1-2H3
InChIKeyUQQROBHFUDBOOK-UHFFFAOYSA-N
SMILESC(=O)C1=CC(OC)=C(OC)C=C1Br
CAS DataBase Reference5392-10-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Safety Statements 24/25
WGK Germany 3
HazardClass IRRITANT
HS Code 29124990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
6-Bromoveratraldehyde Usage And Synthesis
Chemical PropertiesWHITE TO LIGHT YELLOW CRYSTALS OR POWDER
Uses6-Bromoveratraldehyde was used in the preparation of benzylchromenylamines.
Synthesis
Veratraldehyde

120-14-9

6-Bromoveratraldehyde

5392-10-9

(1) Add 529 g of bromine dropwise to 500 g of 3,4-dimethoxybenzaldehyde dissolved in 2.5 L of methanol at room temperature (cooled if necessary) within 1 hour and stir the reaction mixture at the same temperature for 3 hours. Subsequently, 2.5 L of water was slowly added dropwise to the reaction solution to induce precipitation of crystals. A 20% aqueous sodium hydroxide solution was added to the crystal suspension at room temperature and the pH was adjusted to about 9-10, followed by cooling. The precipitated crystals were collected by filtration, washed with water and dried at 50 °C for 12 h. 718.78 g of 6-bromo-3,4-dimethoxybenzaldehyde was finally obtained (yield: 98%).

References[1] Heterocycles, 2015, vol. 90, # 1, p. 730 - 739
[2] Patent: WO2007/40240, 2007, A1. Location in patent: Page/Page column 26
[3] Advanced Synthesis and Catalysis, 2015, vol. 357, # 14-15, p. 3255 - 3261
[4] Patent: EP1964925, 2016, B1. Location in patent: Paragraph 0068
[5] Journal of Asian Natural Products Research, 2012, vol. 14, # 4, p. 322 - 326
Tag:6-Bromoveratraldehyde(5392-10-9) Related Product Information
Veratraldehyde Veratric Acid p-Anisaldehyde 3-(METHOXYMETHOXY)BENZALDEHYDE 2-Bromo-5-methoxybenzaldehyde 3,4-Dimethoxybenzyl alcohol Benzaldehyde Dimethyldimethoxysilane 2,5-Dimethoxybenzaldehyde 2,6-Dimethoxybenzaldehyde 2,4-Dimethoxybenzaldehyde o-Anisaldehyde 2,3-Dimethoxybenzaldehyde 3,5-Dimethoxybenzaldehyde 1,1-Dimethoxyethane 4-Dimethylaminobenzaldehyde Diphenyldimethoxysilane Bromine

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