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ALD01784

Sigma-Aldrich

N-(tert-butyl)-2-methoxypyridin-3-amine

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About This Item

UNSPSC Code:
12352116
PubChem Substance ID:
329772786
NACRES:
NA.22

form

liquid

storage temp.

2-8°C

SMILES string

CC(C)(C)NC1=CC=CN=C1OC

Application

Traditionally challenging to access, this hindered amine provides a chemically differentiated building block for organic synthesis and medicinal chemistry, specifically for preparation of drug candidates containing hindered amine motifs. Additionally, this and over 80 other sterically hindered secondary amines in the Sigma-Aldrich portfolio provide structurally distinct screening compounds. Screen several through Aldrich Market Select. This hindered amine was accessed via a recent publication reported by Baran and coworkers using an innovative hydroamination method.

Other Notes

Product of KemXTree
Practical olefin hydroamination with nitroarenes

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3-((9H-fluoren-2-yl)amino)-3-methylbutan-1-ol

ALD01662

N-(4-(benzyloxy)-2-methylbutan-2-yl)-9H-fluoren-2-amine

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N-(2-methylpentan-2-yl)pyridin-3-amine

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N-(1-(benzyloxy)-2-methylpropan-2-yl)-4-(trifluoromethyl)aniline

ALD01688

4-methoxy-N-(tert-pentyl)aniline

ALD01702

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ALD01736

3-(N-acetyl)-N-(tert-pentyl)aniline

ALD01742

N-(1,1-dimethylethyl)-1-Naphthalenamine

ALD01766

N-(tert-butyl)-4-methoxyaniline

ALD01804

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ALD01818

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ALD00588

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ALD00590

N-(3-(tert-butylamino)phenyl)acetamide

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P301 + P312 + P330

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Related Content

Baran Group – Professor Product Portal

The Baran Group works with Sigma-Aldrich in providing a portfolio of zinc-based reagents promoting difluoromethylation, trifluoromethylation, trifluoroethylation and isopropylation of aryl and heteroaryl motifs. Baran’s lab has also helped introduce a portable desaturase (Tz0Cl), which promotes the installation of alcohol and amine groups and leaves behind a highly useful tosyl group for further transformations.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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