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3-BENZYLOXYBROMOBENZENE

Product Name
3-BENZYLOXYBROMOBENZENE
CAS No.
53087-13-1
Chemical Name
3-BENZYLOXYBROMOBENZENE
Synonyms
Metaraminol Impurity 14;oxy-3-bromobenzene;3-Benzyloxybromobenzen;3-BENZYLOXYBROMOBENZENE;Metaraminol Impurity 29;Metaraminol Impurity 62;3-BROMOPHENYL BENZYL ETHER;1-Bromo-3-benzyloxybenzene;BENZYL 3-BROMOPHENYL ETHER;1-BENZYLOXY-3-BROMOBENZENE
CBNumber
CB6700025
Molecular Formula
C13H11BrO
Formula Weight
263.13
MOL File
53087-13-1.mol
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3-BENZYLOXYBROMOBENZENE Property

Melting point:
57-60 °C
Boiling point:
333.5±17.0 °C(Predicted)
Density 
1.382±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
Solid
color 
White
InChI
InChI=1S/C13H11BrO/c14-12-7-4-8-13(9-12)15-10-11-5-2-1-3-6-11/h1-9H,10H2
InChIKey
HVWZMGZBJCJDOX-UHFFFAOYSA-N
SMILES
C1(Br)=CC=CC(OCC2=CC=CC=C2)=C1
CAS DataBase Reference
53087-13-1(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi,N
Risk Statements 
36/37/38-50/53-43-41
Safety Statements 
26-36/37/39-50/53-43-41-61-60
RIDADR 
UN 3077 9/PG 3
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29093090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H413May cause long lasting harmful effects to aquatic life

Precautionary statements

P273Avoid release to the environment.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
668419
Product name
3-Benzyloxybromobenzene
Purity
96%
Packaging
10g
Price
$84.5
Updated
2023/06/20
Sigma-Aldrich
Product number
668419
Product name
3-Benzyloxybromobenzene
Purity
96%
Packaging
50g
Price
$216
Updated
2023/06/20
TCI Chemical
Product number
B2307
Product name
1-Benzyloxy-3-bromobenzene
Purity
>98.0%(GC)
Packaging
5g
Price
$34
Updated
2025/07/31
TCI Chemical
Product number
B2307
Product name
1-Benzyloxy-3-bromobenzene
Purity
>98.0%(GC)
Packaging
25g
Price
$134
Updated
2025/07/31
TRC
Product number
B291410
Product name
1-(Benzyloxy)-3-bromobenzene
Packaging
2.5g
Price
$65
Updated
2021/12/16
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3-BENZYLOXYBROMOBENZENE Chemical Properties,Usage,Production

Chemical Properties

Whitetolightyellowcrystalpowde

Synthesis

591-20-8

100-44-7

53087-13-1

1. Anhydrous potassium carbonate (37.32 g, 270 mmol) and benzyl chloride (11.50 mL, 99 mmol) were added to a suspension of anhydrous ethanol (300 mL) containing m-bromophenol (15.57 g, 90 mmol) under nitrogen protection. The reaction mixture was heated to reflux for 4 hours. After completion of the reaction, the ethanol was removed by vacuum filtration and evaporation. The residue was extracted with ethyl acetate (EtOAc) and the combined organic layers were washed sequentially with water, 2 M NaOH solution, saturated brine and 2 M HCl solution, dried over anhydrous sodium sulfate (Na2SO4) and concentrated to give the yellow solid product 3-benzyloxybromobenzene (22.02 g, 93%). 2. To a 250 mL two-necked round-bottomed flask, protected by nitrogen, were added dry magnesium chips (2.18 g, 90 mmol) and trace iodine, equipped with two rubber septa and stirred. Anhydrous tetrahydrofuran (THF, 40 mL) solution of 3-benzyloxybromobenzene (15.79 g, 60 mmol) was slowly added through a syringe and kept at reflux. After addition, stirring was continued at reflux for 5 hours. After the reaction mixture was cooled to -30°C, anhydrous THF (60 mL) solution of trimethyl borate (9.36 g, 90 mmol) was slowly added. After addition, the mixture was stirred at room temperature overnight, followed by treatment with saturated ammonium chloride (NH4Cl) solution and continued stirring at room temperature for 1 hour. THF was removed by rotary evaporation, the aqueous layer was extracted with EtOAc, dried over anhydrous Na2SO4, filtered and concentrated to give a yellow crude product. The crude product was purified by recrystallization in water to give white solid target product (7.53 g, 55%).

References

[1] Journal of Materials Chemistry, 2010, vol. 20, # 15, p. 3069 - 3078
[2] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 5, p. 1044 - 1054
[3] Journal of Medicinal and Pharmaceutical Chemistry, 1962, vol. 5, p. 752 - 762
[4] Patent: US5447656, 1995, A
[5] Patent: EP838461, 1998, A2

3-BENZYLOXYBROMOBENZENE Preparation Products And Raw materials

Raw materials

Preparation Products

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3-BENZYLOXYBROMOBENZENE Suppliers

TCI Europe
Tel
320-37350700
Fax
+32 (0)37350701
Email
sales@tcieurope.eu
Country
Europe
ProdList
23671
Advantage
75
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View Lastest Price from 3-BENZYLOXYBROMOBENZENE manufacturers

Shaanxi Dideu New Materials Co. Ltd
Product
3-BENZYLOXYBROMOBENZENE 53087-13-1
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98.0%
Supply Ability
10000KGS
Release date
2025-03-07
Career Henan Chemical Co
Product
3-BENZYLOXYBROMOBENZENE 53087-13-1
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
200kg
Release date
2018-12-25

53087-13-1, 3-BENZYLOXYBROMOBENZENERelated Search:


  • 1-BENZYLOXY-3-BROMOBENZENE
  • 1-Benzyloxy-3-broMobenzene,Benzyl 3-BroMophenyl Ether
  • BENZYL 3-BROMOPHENYL ETHER
  • 3-Benzyloxybromobenzen
  • 1-Bromo-3-benzyloxybenzene
  • 3-BROMOPHENYL BENZYL ETHER
  • 3-BENZYLOXYBROMOBENZENE
  • 1-(Benzyloxy)-3-bromobenzen
  • oxy-3-bromobenzene
  • 1-Benzyloxy-3-bromobenzene &gt
  • Benzene, 1-bromo-3-(phenylmethoxy)-
  • Metaraminol Impurity 14
  • 1-Benzyloxy-3-bromobzenzene
  • (E)-1-(3-(benzyloxy)phenyl)-1-hydroxypropan-2-one oxime
  • Metaraminol Impurity 29
  • Metaramine bitartrate Impurity 33
  • Metaraminol Impurity 62
  • Metaraminol Bitartrate Impurity 83
  • 53087-13-1
  • Ethers
  • Organic Building Blocks
  • Oxygen Compounds
  • Building Blocks
  • Phenetole
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Bromine Compounds
  • Ethers
  • Organic Building Blocks
  • Oxygen Compounds
  • alkyl bromide