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2-(4-BroMo-2-Methylphenyl)acetonitrile

Product Name
2-(4-BroMo-2-Methylphenyl)acetonitrile
CAS No.
215800-05-8
Chemical Name
2-(4-BroMo-2-Methylphenyl)acetonitrile
Synonyms
4-Bromo-2-methylbenzyl cyanide;4-broMo-2-Methylphenylacetonitrile;Benzeneacetonitrile, 4-bromo-2-methyl-;2-(4-BroMo-2-Methylphenyl)acetonitrile
CBNumber
CB82665452
Molecular Formula
C9H8BrN
Formula Weight
210.07
MOL File
215800-05-8.mol
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2-(4-BroMo-2-Methylphenyl)acetonitrile Property

Boiling point:
305.7±27.0 °C(Predicted)
Density 
1.418±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to yellow Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

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
B614330
Product name
2-(4-Bromo-2-methylphenyl)acetonitrile
Packaging
50mg
Price
$45
Updated
2021/12/16
TRC
Product number
B614330
Product name
2-(4-Bromo-2-methylphenyl)acetonitrile
Packaging
100mg
Price
$60
Updated
2021/12/16
Matrix Scientific
Product number
126529
Product name
2-(4-Bromo-2-methylphenyl)acetonitrile
Purity
>95%
Packaging
1g
Price
$288
Updated
2021/12/16
AK Scientific
Product number
0971AB
Product name
2-(4-Bromo-2-methylphenyl)acetonitrile
Packaging
10g
Price
$436
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0362632
Product name
2-(4-BROMO-2-METHYLPHENYL)ACETONITRILE
Purity
95.00%
Packaging
5MG
Price
$500.59
Updated
2021/12/16
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2-(4-BroMo-2-Methylphenyl)acetonitrile Chemical Properties,Usage,Production

Synthesis

143-33-9

156001-49-9

215800-05-8

Step c: Synthesis of intermediate 5,2-(4-bromo-2-methylphenyl)acetonitrile 1-Bromo-4-(bromomethyl)-3-methylbenzene (13.2 g, 50.1 mmol) was dissolved in DMF (65 mL). The reaction mixture was cooled to 0-5 °C, followed by addition of NaCN (3.66 g, 74.6 mmol) and water (8 mL). The reaction mixture was stirred at room temperature overnight. After completion of the reaction, water (170 mL) and saturated NaHCO3 solution (130 mL) were added, followed by hexane/Et2O (2:1, 150 mL) for extraction. The organic phase was separated and the aqueous phase was further extracted with hexane/Et2O (2:1, 3 x 150 mL). All organic phases were combined, washed with water (170 mL), dried over MgSO4, filtered and concentrated under reduced pressure to afford the target product 2-(4-bromo-2-methylphenyl)acetonitrile (9.76 g, 93% yield) as an orange oil. 1H NMR (300 MHz, chloroform-D) δ: 7.40-7.32 (2H, m), 7.23 (2H, d, J = 8.2 Hz), 3.61 (2H, s), 2.32 (3H, s).

References

[1] Patent: WO2008/18827, 2008, A1. Location in patent: Page/Page column 61-62
[2] Patent: WO2006/18725, 2006, A1. Location in patent: Page/Page column 164

2-(4-BroMo-2-Methylphenyl)acetonitrile Preparation Products And Raw materials

Raw materials

Preparation Products

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2-(4-BroMo-2-Methylphenyl)acetonitrile Suppliers

Energy Chemical
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021-021-58432009 400-005-6266
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China
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China
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215800-05-8, 2-(4-BroMo-2-Methylphenyl)acetonitrileRelated Search:


  • 2-(4-BroMo-2-Methylphenyl)acetonitrile
  • 4-broMo-2-Methylphenylacetonitrile
  • 4-Bromo-2-methylbenzyl cyanide
  • Benzeneacetonitrile, 4-bromo-2-methyl-
  • 215800-05-8