3,5-Dibromoanisole

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Products Intro: Product Name:3,5-Dibromoanisole
CAS:74137-36-3
Purity:98%(Min, GC ) Package:1G;1KG;100KG
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Products Intro: Product Name:3,5-Dibromoanisole
CAS:74137-36-3
Purity:99% Package:25KG;5KG;1KG
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Products Intro: Product Name:3,5-Dibromoanisole
CAS:74137-36-3
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:3,5-Dibromoanisole
CAS:74137-36-3
Company Name: Standardpharm Co. Ltd.
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Products Intro: Product Name:Phloroglucinol Impurity 13
CAS:74137-36-3
Purity:0.99 Package:10mg;25mg;50mg;100mg

3,5-Dibromoanisole manufacturers

  • 3,5-Dibromoanisole
  • 3,5-Dibromoanisole pictures
  • $1.00
  • 2019-12-26
  • CAS:74137-36-3
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 500kg
3,5-Dibromoanisole Basic information
Product Name:3,5-Dibromoanisole
Synonyms:3,5-DIBROMOANISOLE;Benzene,1,3-dibroMo-5-Methoxy-;Phloroglucinol Impurity 13;3,5-dibromophenyl ether;3,5-Dibromoanisole>;3,5-DibromoanisoL;3,5-Dibromobenzyl ether;1,3-dibromo-5-methoxybenzene
CAS:74137-36-3
MF:C7H6Br2O
MW:265.93
EINECS:
Product Categories:Multisubstituted Benzene;Anisole;Ethers;Organic Building Blocks;Oxygen Compounds
Mol File:74137-36-3.mol
3,5-Dibromoanisole Structure
3,5-Dibromoanisole Chemical Properties
Melting point 34-38 °C
Boiling point 249.7°C
density 1.823
Fp 98.1°C
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
color White to Gray to Brown
Stability:Stable. Incompatible with strong oxidizing agents.
InChIInChI=1S/C7H6Br2O/c1-10-7-3-5(8)2-6(9)4-7/h2-4H,1H3
InChIKeyOQZAQBGJENJMHT-UHFFFAOYSA-N
SMILESC1(Br)=CC(OC)=CC(Br)=C1
CAS DataBase Reference74137-36-3(CAS DataBase Reference)
Safety Information
Hazard Codes T
Risk Statements 25
Safety Statements 45
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
HazardClass 6.1
PackingGroup 
HS Code 2909303890
MSDS Information
3,5-Dibromoanisole Usage And Synthesis
Chemical Propertiessolid
Uses3,5-Dibromoanisole, is an organic building block used for the synthesis of various pharmaceutical compounds, such as Dicationic m-Terphenyl and 1,3-Dipyridylbenzene Derivatives, having Antiprotozoal Activity.
Synthesis
Methanol

67-56-1

3,5-DIBROMONITRO BENZENE

6311-60-0

3,5-Dibromoanisole

74137-36-3

The general procedure for the synthesis of 3,5-dibromoanisole from methanol and 1,3-dibromo-5-nitrobenzene was as follows: 1,3-dibromo-5-nitrobenzene (21.07 g, 75 mmol), freshly powdered potassium hydroxide (7.57 g, 135 mmol) and tetrabutyl ammonium bromide (2.42 g, 7.5 mmol) were suspended in tetramethylurea (80 mL). A solution of methanol (4.81 g, 6.09 mL, 150 mmol) dissolved in 20 mL of tetramethylurea was added slowly and dropwise to the above brown suspension over a period of 15 min at room temperature. The reaction mixture was stirred continuously for 24 h at room temperature before it was quenched by pouring it into ice (150 g) and extracted with tert-butyl methyl ether (3 x 250 mL). The organic phases were combined, dried with magnesium sulfate and subsequently concentrated under reduced pressure to give the crude product. The crude product was purified by reduced pressure distillation (124 °C, 10 Torr) to give 16.74 g (84% yield) of 3,5-dibromoanisole as a light yellow solid.

References[1] Patent: US2006/270686, 2006, A1. Location in patent: Page/Page column 35
[2] Journal of Medicinal Chemistry, 2011, vol. 54, # 1, p. 179 - 200
[3] Patent: US2008/280891, 2008, A1. Location in patent: Page/Page column 34-35
[4] Patent: WO2008/8059, 2008, A1. Location in patent: Page/Page column 96
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