2-BROMO-5-METHOXYBENZYL BROMIDE 97

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Products Intro: Product Name:2-BROMO-5-METHOXYBENZYL BROMIDE
CAS:19614-12-1
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Products Intro: Product Name:4-Bromo-3-bromomethyl anisole
CAS:19614-12-1
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CAS:19614-12-1
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2-BROMO-5-METHOXYBENZYL BROMIDE 97 manufacturers

2-BROMO-5-METHOXYBENZYL BROMIDE 97 Basic information
Product Name:2-BROMO-5-METHOXYBENZYL BROMIDE 97
Synonyms:2-bromo-5-methoxybromobenzyl;5-BroMo-2-Methoxy Benzyl BroMide;2-BROMO-5-METHOXYBENZYL BROMIDE 97;4-Bromo-3-bromomethyl anisole;2-Bromo-5-methyoxybenzyl bromide;2-Bromo-5-methoxybenzyl bromide 97%;2-Bromo-5-methoxybenzyl Bromide >;Benzene, 1-bromo-2-(bromomethyl)-4-methoxy-
CAS:19614-12-1
MF:C8H8Br2O
MW:279.96
EINECS:
Product Categories:Building Blocks;C2 to C8;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Ethers;Organic Building Blocks;Oxygen Compounds;alkyl bromide
Mol File:19614-12-1.mol
2-BROMO-5-METHOXYBENZYL BROMIDE  97 Structure
2-BROMO-5-METHOXYBENZYL BROMIDE 97 Chemical Properties
Melting point 90-94 °C (lit.)
Boiling point 299.6±25.0 °C(Predicted)
density 1.759±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Solid
color White to beige
Water Solubility Soluble in hot methanol. Slightly soluble in water.
InChIInChI=1S/C8H8Br2O/c1-11-7-2-3-8(10)6(4-7)5-9/h2-4H,5H2,1H3
InChIKeyMURVUTUZSUEIGI-UHFFFAOYSA-N
SMILESC1(Br)=CC=C(OC)C=C1CBr
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR UN 3261 8/PG 2
WGK Germany 3
HazardClass 8
PackingGroup 
HS Code 2909303890
MSDS Information
2-BROMO-5-METHOXYBENZYL BROMIDE 97 Usage And Synthesis
UsesEmployed as an important intermediate for raw material for organic synthesis, agrochemical, pharmaceutical and dyestuff field
Synthesis
2-Bromo-5-methoxytoluene

27060-75-9

2-BROMO-5-METHOXYBENZYL BROMIDE  97

19614-12-1

The general procedure for the synthesis of 2-bromo-5-methoxybenzyl bromide from 2-bromo-5-methoxytoluene was as follows: 2-bromo-5-methoxytoluene (0.050 mol) and N-bromosuccinimide (NBS, 0.055 mol) were dissolved in carbon tetrachloride (125 mL), and azobisisobutyronitrile (AIBN, 0.001 mol) was added as initiator. The reaction mixture was stirred at 80 °C for 18 hours. Upon completion of the reaction, the mixture was diluted with hexane and subsequently filtered through a diatomaceous earth pad to remove insoluble impurities. The filtrate was concentrated under reduced pressure to remove the solvent and the residue was washed with ethyl acetate to give the final target product 4-bromo-3-(bromomethyl)anisole.

References[1] Tetrahedron, 2004, vol. 60, # 49, p. 11075 - 11087
[2] Journal of the American Chemical Society, 2005, vol. 127, # 29, p. 10124 - 10125
[3] Journal of Organic Chemistry, 2014, vol. 79, # 11, p. 4973 - 4983
[4] Synlett, 2011, # 17, p. 2525 - 2528
[5] Journal of Medicinal Chemistry, 2000, vol. 43, # 1, p. 22 - 26
Tag:2-BROMO-5-METHOXYBENZYL BROMIDE 97(19614-12-1) Related Product Information
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