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2-(5-Methylpyridin-2-yl)acetonitrile

Product Name
2-(5-Methylpyridin-2-yl)acetonitrile
CAS No.
38203-08-6
Chemical Name
2-(5-Methylpyridin-2-yl)acetonitrile
Synonyms
5-methyl-2-pyridineacetonitrile;2-Pyridineacetonitrile, 5-methyl-;2-(5-Methylpyridin-2-yl)acetonitrile;1-[2-[4-[(3R,4R)-7-methoxy-3-phenyl-3,4-dihydro-2H-1-benzopyran-4-yl]phenoxy]ethyl]pyrrolidine
CBNumber
CB92552274
Molecular Formula
C8H8N2
Formula Weight
132.16
MOL File
38203-08-6.mol
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2-(5-Methylpyridin-2-yl)acetonitrile Property

Boiling point:
105-106 °C(Press: 3 Torr)
Density 
1.056±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
3.47±0.22(Predicted)
Appearance
Light yellow to yellow Liquid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

AK Scientific
Product number
6422CC
Product name
2-(5-Methylpyridin-2-yl)acetonitrile
Packaging
250mg
Price
$141
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0381142
Product name
2-(5-METHYLPYRIDIN-2-YL)ACETONITRILE
Purity
95.00%
Packaging
5MG
Price
$499.3
Updated
2021/12/16
Alichem
Product number
38203086
Product name
5-Methylpyridine-2-acetonitrile
Packaging
1g
Price
$572.57
Updated
2021/12/16
Ambeed
Product number
A450564
Product name
2-(5-Methylpyridin-2-yl)acetonitrile
Purity
95%
Packaging
100mg
Price
$22
Updated
2021/12/16
Ambeed
Product number
A450564
Product name
2-(5-Methylpyridin-2-yl)acetonitrile
Purity
95%
Packaging
250mg
Price
$43
Updated
2021/12/16
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2-(5-Methylpyridin-2-yl)acetonitrile Chemical Properties,Usage,Production

Synthesis

3510-66-5

38203-08-6

Step 3 - Preparation of 2-(5-methylpyridin-2-yl)acetonitrile: To a solution of anhydrous acetonitrile (10.1 mL, 191.83 mmol, 3.3 eq.) in anhydrous tetrahydrofuran (500 mL) was added slowly and dropwise at -78 °C a solution of n-butyllithium (2.5 M, 69.8 mL, 174.39 mmol, 3 eq.) in hexanes, protected by nitrogen. The resulting white suspension was stirred at -78 °C for 1 h. Anhydrous tetrahydrofuran (30 mL) solution of 2-bromo-5-methylpyridine (10.0 g, 58.13 mmol, 1 eq.) was added. The reaction mixture was kept at -78 °C for 1 h, followed by a slow warming to room temperature and continued stirring for 1 h. The reaction was completed by the addition of ice water. Upon completion of the reaction, the reaction was quenched by the addition of ice water and layered. The organic layer was washed sequentially with water and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 18 g of crude product. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate=15:1) to afford 2-(5-methylpyridin-2-yl)acetonitrile (6.2 g, 80% yield).1H NMR (300 MHz, CDCl3): δ 8.40 (d, J=3.0 Hz, 1H), 7.54 (dd, J1=3.0 Hz, J2=6.0 Hz. 1H), 7.32 (d, J=6.0 Hz, 1H), 3.90 (s, 2H), 2.40 (s, 3H).

References

[1] Patent: US2009/280230, 2009, A1
[2] Patent: US2009/280230, 2009, A1
[3] Patent: US2009/280230, 2009, A1

2-(5-Methylpyridin-2-yl)acetonitrile Preparation Products And Raw materials

Raw materials

Preparation Products

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2-(5-Methylpyridin-2-yl)acetonitrile Suppliers

Synthonix Inc
Tel
--
Fax
--
Email
info@synthonix.com
Country
United States
ProdList
6872
Advantage
58
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80

38203-08-6, 2-(5-Methylpyridin-2-yl)acetonitrileRelated Search:


  • 2-(5-Methylpyridin-2-yl)acetonitrile
  • 5-methyl-2-pyridineacetonitrile
  • 1-[2-[4-[(3R,4R)-7-methoxy-3-phenyl-3,4-dihydro-2H-1-benzopyran-4-yl]phenoxy]ethyl]pyrrolidine
  • 2-Pyridineacetonitrile, 5-methyl-
  • 38203-08-6