91419-52-2
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 |
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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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