1-N-Cbz-4-cyanopiperidine
- Product Name
- 1-N-Cbz-4-cyanopiperidine
- CAS No.
- 161609-84-3
- Chemical Name
- 1-N-Cbz-4-cyanopiperidine
- Synonyms
- BUTTPARK 93\50-50;1-Z-4-cyanopiperidine;1-CBZ-4-CYANOPIPERIDINE;N-CBZ-4-cyanopiperidine;1-N-CBZ-4-CYANO-PIPERIDINE;1-N-Cbz-4-cycano-piperidine;1-N-CBZ-PIPERIDINE-4-CARBONITRILE;4-Cyanopiperidine, N-CBZ protected;BENZYL-4-CYANOPIPERIDINE-1-CARBOXYLATE;4-CYANO-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER
- CBNumber
- CB7763001
- Molecular Formula
- C14H16N2O2
- Formula Weight
- 244.29
- MOL File
- 161609-84-3.mol
1-N-Cbz-4-cyanopiperidine Property
- Boiling point:
- 416.5±45.0 °C(Predicted)
- Density
- 1.18±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- -3.13±0.40(Predicted)
- Appearance
- White to off-white Solid
Safety
- HS Code
- 29333990
N-Bromosuccinimide Price
- Product number
- B194155
- Product name
- Benzyl4-cyanopiperidine-1-carboxylate
- Packaging
- 250mg
- Price
- $55
- Updated
- 2021/12/16
- Product number
- J56774
- Product name
- 1-N-Cbz-4-Cyanopiperidine
- Packaging
- 5g
- Price
- $55
- Updated
- 2021/12/16
- Product number
- FB140315
- Product name
- Benzyl 4-cyanopiperidine-1-carboxylate
- Packaging
- 5G
- Price
- $167
- Updated
- 2021/12/16
- Product number
- W3511
- Product name
- 1-N-Cbz-4-Cyanopiperidine
- Packaging
- 25g
- Price
- $254
- Updated
- 2021/12/16
- Product number
- FB140315
- Product name
- Benzyl 4-cyanopiperidine-1-carboxylate
- Packaging
- 10g
- Price
- $290
- Updated
- 2021/12/16
1-N-Cbz-4-cyanopiperidine Chemical Properties,Usage,Production
Synthesis
167757-45-1
161609-84-3
General procedure for the synthesis of 1-N-Cbz-4-cyanopiperidine from 1-Cbz-piperidine-4-carboxamide: 1-Cbz-piperidine-4-carboxamide (1.0 mmol) and triethylamine (Et3N, 1.5 mmol) were dissolved in ethyl acetate (EtOAc, 1 mL, 1 M) at room temperature. Subsequently, XtalFluor-E (1.1 mmol) was added in batches. The reaction mixture was stirred at room temperature for 1 hour. Upon completion of the reaction, the reaction was quenched with saturated sodium bicarbonate (NaHCO3) solution. Next, the reaction mixture was washed with aqueous sodium carbonate (Na2CO3) solution and extracted with dichloromethane (CH2Cl2, 2 × 10 mL). The organic layers were combined, washed sequentially with water and brine, dried over anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure to give the crude product. If necessary, the crude product can be purified by fast column chromatography.
References
[1] Synthesis (Germany), 2015, vol. 47, # 23, p. 3758 - 3766
1-N-Cbz-4-cyanopiperidine Preparation Products And Raw materials
Raw materials
Preparation Products
1-N-Cbz-4-cyanopiperidine Suppliers
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- Canada
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