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3-Bromo-4-methoxybenzonitrile

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Products Intro: Product Name:3-Bromo-4-methoxybenzonitrile
CAS:117572-79-9
Purity:98%(Min,HPLC) Package:1G;1KG;100KG
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Products Intro: Product Name:3-bromo-4-methoxybenzonitrile
CAS:117572-79-9
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
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CAS: 117572-79-9
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Products Intro: Product Name:3-Bromo-4-methoxybenzonitrile
CAS:117572-79-9
Purity:>97% Package:1g;5g;10g;25g;100g;500g

3-Bromo-4-methoxybenzonitrile manufacturers

3-Bromo-4-methoxybenzonitrile Basic information
Product Name:3-Bromo-4-methoxybenzonitrile
Synonyms:3-BROMO-4-METHOXYBENZONITRILE;3-BROMO-4-METHOXYBENZOTRIFLUORIDE;2-METHOXY-5-(TRIFLUOROMETHYL)BROMOBENZENE;BUTTPARK 87\07-61;AKOS B004290;3-Bromo-p-anisyl cyanide;2-Bromo-4-(trifluoromethyl)anisole;2-Bromo-4-cyanoanisole
CAS:117572-79-9
MF:C8H6BrNO
MW:212.04
EINECS:601-486-2
Product Categories:Aromatic Nitriles;Nitrile;Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds;Nitriles;C8 to C9;Cyanides/Nitriles;Nitrogen Compounds
Mol File:117572-79-9.mol
3-Bromo-4-methoxybenzonitrile Structure
3-Bromo-4-methoxybenzonitrile Chemical Properties
Melting point 122-124 °C (lit.)
Boiling point 282.8±20.0 °C(Predicted)
density 1.56±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Soluble in methanol.
form powder to crystal
color White to Light yellow to Light orange
BRN 3246576
CAS DataBase Reference117572-79-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38-52
Safety Statements 26-36
RIDADR 3439
WGK Germany 3
Hazard Note Harmful/Irritant
HazardClass 6.1
PackingGroup III
HS Code 29269090
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
3-Bromo-4-methoxybenzonitrile Usage And Synthesis
Chemical PropertiesOff-white powder
Uses3-Bromo-4-methoxybenzonitrile is used to prepare 3-bromo-2-iodo-4-methoxy-benzonitrile. It is also used as pharmaceutical intermediates.
Synthesis
3-BROMO-4-HYDROXYBENZONITRILE

2315-86-8

Iodomethane

74-88-4

3-Bromo-4-methoxybenzonitrile

117572-79-9

The reaction was carried out with 3-bromo-4-hydroxybenzonitrile (5.0 g, 25.3 mmol), potassium carbonate (7.0 g, 50.1 mmol) and iodomethane (3.9 g, 27.8 mmol) in acetonitrile (20 mL) with stirring for 6 h at 25 °C. The reaction was carried out by thin layer chromatography (TLC). The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the reaction mixture was subjected to liquid-liquid separation between ethyl acetate (100 mL) and water (30 mL). The organic phase was collected, washed with brine (20 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain the crude product. The crude product was purified by fast column chromatography on silica gel to afford 3-bromo-4-methoxybenzenecarbonitrile (4.8 g, 22.6 mmol) in 89% yield using a hexane solution of 30% ethyl acetate as eluent.

References[1] Patent: WO2017/11590, 2017, A1. Location in patent: Paragraph 00409
[2] Patent: US2005/153877, 2005, A1. Location in patent: Page/Page column 122
3-Bromo-4-methoxybenzonitrile Preparation Products And Raw materials
Raw materials3-BROMO-4-HYDROXYBENZONITRILE-->Iodomethane-->Potassium carbonate-->Acetonitrile
Preparation Products3-BROMO-4-METHOXYBENZYLAMINE-->5-(3-BROMO-4-METHOXY-PHENYL)-2H-TETRAZOLE
Tag:3-Bromo-4-methoxybenzonitrile(117572-79-9) Related Product Information
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