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5-(1-Methylethyl)-2-pyridinamine

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Products Intro: Product Name:5-(1-Methylethyl)-2-pyridinamine
CAS:603310-75-4
Purity:NLT 98% Package:1G;1KG;100KG
Company Name: Zhejiang ZETian Fine Chemicals Co. LTD
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Products Intro: Product Name:5-(1-Methylethyl)-2-pyridinamine
CAS:603310-75-4
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:5-(1-Methylethyl)-2-pyridinamine
CAS:603310-75-4
Purity:98% HPLC LCMS Package:10G;20G
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:5-Isopropylpyridin-2-amine
CAS:603310-75-4
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-56290
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Products Intro: Product Name:5-(1-Methylethyl)-2-pyridinamine
CAS:603310-75-4
Purity:95-99% Package:1KG;1USD

5-(1-Methylethyl)-2-pyridinamine manufacturers

5-(1-Methylethyl)-2-pyridinamine Basic information
Uses
Product Name:5-(1-Methylethyl)-2-pyridinamine
Synonyms:2-PYRIDINAMINE, 5-(1-METHYLETHYL)-;5-(1-Methylethyl)-2-Pyridinamine;2-Pyridinamine,5-(1-methylethyl)-(9CI);2-AMino-5-isopropylpyridine;5-(propan-2-yl)pyridin-2-aMine;(5-Isopropylpyridin-2-yl)amine;2-amino-5-(propan-2-yl)pyridine
CAS:603310-75-4
MF:C8H12N2
MW:136.19
EINECS:200-258-5
Product Categories:Heterocycle-Pyridine series;PYRIDINE
Mol File:603310-75-4.mol
5-(1-Methylethyl)-2-pyridinamine Structure
5-(1-Methylethyl)-2-pyridinamine Chemical Properties
Boiling point 253 ºC
density 1.008
Fp 130 ºC
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka6.95±0.13(Predicted)
AppearanceLight yellow to brown Solid-liquid mixture
Safety Information
RIDADR UN2810
HazardClass 6.1
MSDS Information
5-(1-Methylethyl)-2-pyridinamine Usage And Synthesis
Uses5-Isopropylpyridine-2-amine can be used as a pharmaceutical synthesis intermediate.
Synthesis
2-Nitro-5-(prop-1-en-2-yl)pyridine

1135437-90-9

5-(1-Methylethyl)-2-pyridinamine

603310-75-4

Step B: Synthesis of 5-isopropylpyridin-2-amine as an intermediate; [0209] A mixture of 2-nitro-5-(prop-1-en-2-yl)pyridine (0.104 g, 0.63 mmol) with 10% palladium-carbon catalyst (0.011 g, 10 wt%) in ethanol (10 mL) was subjected to a hydrogen atmosphere and stirred at atmospheric pressure for overnight reaction. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration and the filtrate was concentrated under reduced pressure to give 5-isopropylpyridin-2-amine (0.120 g, 139% yield) as an oily product. Its structure was confirmed by 1H NMR (500 MHz, CDCl3): δ 7.68 (d, J = 8.1 Hz, 1H), 7.51 (s, 1H), 7.48 (s, 2H), 7.14 (d, J = 9.1 Hz, 1H), 3.45-3.42 (m, 1H), 1.38 (d, J = 8.6 Hz, 6H); ESI MS m/z 137 [M + H]+.

References[1] Patent: WO2009/42907, 2009, A1. Location in patent: Page/Page column 83
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