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2-Bromo-6-methoxybenzonitrile

Product Name
2-Bromo-6-methoxybenzonitrile
CAS No.
1245647-50-0
Chemical Name
2-Bromo-6-methoxybenzonitrile
Synonyms
2-Bromo-6-methoxybenzonitrile;Benzonitrile, 2-bromo-6-methoxy-
CBNumber
CB52500020
Molecular Formula
C8H6BrNO
Formula Weight
212.04
MOL File
1245647-50-0.mol
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2-Bromo-6-methoxybenzonitrile Property

Boiling point:
310.9±27.0 °C(Predicted)
Density 
1.56±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
color 
Pale yellow
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Safety

HS Code 
2926907090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
B696603
Product name
2-Bromo-6-methoxybenzonitrile
Packaging
250mg
Price
$55
Updated
2021/12/16
AK Scientific
Product number
X9592
Product name
2-Bromo-6-methoxybenzonitrile
Packaging
250mg
Price
$81
Updated
2021/12/16
AK Scientific
Product number
X9592
Product name
2-Bromo-6-methoxybenzonitrile
Packaging
1g
Price
$95
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0357650
Product name
2-BROMO-6-METHOXYBENZONITRILE
Purity
95.00%
Packaging
5MG
Price
$502.36
Updated
2021/12/16
Ambeed
Product number
A122547
Product name
2-Bromo-6-methoxybenzonitrile
Purity
98%
Packaging
250mg
Price
$16
Updated
2021/12/16
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2-Bromo-6-methoxybenzonitrile Chemical Properties,Usage,Production

Synthesis

1393739-62-2

1245647-50-0

The general procedure for the synthesis of 2-bromo-6-methoxybenzonitrile using the compound (CAS:1393739-62-2) as starting material was as follows: 1-(azidomethyl)-4-methoxybenzene (8a) (81 mg, 0.5 mmol) was dissolved in acetonitrile (0.5 mL) at 0 °C followed by the addition of iodobenzene dibenzoate (PhI(OAc)2) ( 483.1 mg, 1.5 mmol). A solution of tert-butyl hydroperoxide (tBuOOH) (5.0-6.0 M, dissolved in decane, 360 μL, 2.0 mmol) was slowly added dropwise over a period of 1 h under vigorous stirring. After dropwise addition, stirring of the reaction mixture was continued for 11 hours. Upon completion of the reaction, the target product 4-methoxybenzyl cyanide (9a) was purified by silica gel column chromatography using hexane/ethyl acetate (10:1) as eluent to give the target product 4-methoxybenzonitrile (9a) as a yellow oil (55.3 mg, 83% yield).

References

[1] Tetrahedron Letters, 2012, vol. 53, # 35, p. 4766 - 4769

2-Bromo-6-methoxybenzonitrile Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Bromo-6-methoxybenzonitrile Suppliers

Shanghai Hanhong Scientific Co.,Ltd.
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021-54306202 13764082696
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China
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1245647-50-0, 2-Bromo-6-methoxybenzonitrileRelated Search:


  • 2-Bromo-6-methoxybenzonitrile
  • Benzonitrile, 2-bromo-6-methoxy-
  • 1245647-50-0