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91419-52-2

91419-52-2 structural image
Product Name: 1-Boc-4-cyanopiperidine
Formula: C11H18N2O2
Synonyms: 1,1-Dimethylethyl 4-cyano-1-piperidinecarboxylate;1-Boc-4-cyanopiperidine;4-Cyano-1-piperidinecarboxylic acid 1,1-dimethylethyl ester
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SAFETY INFORMATION

Signal word Warning
Pictogram(s)

Skull and Crossbones
Acute Toxicity
GHS06

Exclamation Mark
Irritant
GHS07

Environment
GHS09
GHS Hazard Statements H302:Acute toxicity,oral
H312:Acute toxicity,dermal
H315:Skin corrosion/irritation
H319:Serious eye damage/eye irritation
H331:Acute toxicity,inhalation
H400:Hazardous to the aquatic environment, acute hazard
Precautionary Statement Codes P261:Avoid breathing dust/fume/gas/mist/vapours/spray.
P264:Wash hands thoroughly after handling.
P264:Wash skin thouroughly after handling.
P270:Do not eat, drink or smoke when using this product.
P271:Use only outdoors or in a well-ventilated area.
P273:Avoid release to the environment.
P280:Wear protective gloves/protective clothing/eye protection/face protection.
P304+P340:IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405:Store locked up.
P403+P233:Store in a well-ventilated place. Keep container tightly closed.
P501:Dispose of contents/container to..…

COMPUTED DESCRIPTORS

Molecular Weight 210.27 g/mol
XLogP3 1.3
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 2
Exact Mass 210.136827821 g/mol
Monoisotopic Mass 210.136827821 g/mol
Topological Polar Surface Area 53.3 Ų
Heavy Atom Count 15
Formal Charge 0
Complexity 277
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

PRODUCT INTRODUCTION

Description

1-Boc-4-cyanopiperidine is an organic heterocyclic compound, which can be used as pharmaceutical intermediates. The synthesis of 1-Boc-4-cyanopiperidine is through the dehydration of oximes and amides to nitriles. The solution of the aldoxime and XtalFluor-E8 is mixed to extract with CH2Cl2 (2 × 10 mL), The combined organic layers were washed, dried, and concentrated under vacuum to afford the crude nitrile, which was purified by flash chromatography, if required.

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