Benzyl 4-hydroxy-1-piperidinecarboxylate
- Product Name
- Benzyl 4-hydroxy-1-piperidinecarboxylate
- CAS No.
- 95798-23-5
- Chemical Name
- Benzyl 4-hydroxy-1-piperidinecarboxylate
- Synonyms
- BENZYL 4-HYDROXYPIPERIDINE-1-CARBOXYLATE;BUTTPARK 93\50-53;1-Cbz-4-piperidinol;1-CBZ-4-hydroxypethidine;1-Cbz-4-hydroxypiperidine;N-CBZ-4-HYDROXYPIPERIDINE;N-CBZ-4-HYDROXY-1-PIPERIDINE;1-Carbobenzoxy-4-piperidinol;1-Carbobenzoxy-4-hydroxypiperidine;1-(Benzyloxycarbonyl)-4-piperidinol
- CBNumber
- CB5199534
- Molecular Formula
- C13H17NO3
- Formula Weight
- 235.28
- MOL File
- 95798-23-5.mol
Benzyl 4-hydroxy-1-piperidinecarboxylate Property
- Boiling point:
- 167 °C/0.2 mmHg (lit.)
- Density
- 1.554 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.543(lit.)
- Flash point:
- >230 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- Oil
- pka
- 14.79±0.20(Predicted)
- color
- Orange
- InChI
- InChI=1S/C13H17NO3/c15-12-6-8-14(9-7-12)13(16)17-10-11-4-2-1-3-5-11/h1-5,12,15H,6-10H2
- InChIKey
- JKIUUDJOCYHIGY-UHFFFAOYSA-N
- SMILES
- N1(C(OCC2=CC=CC=C2)=O)CCC(O)CC1
- CAS DataBase Reference
- 95798-23-5(CAS DataBase Reference)
Safety
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- WGK Germany
- 3
- Hazard Note
- Irritant
- HS Code
- 2933399990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 513903
- Product name
- Benzyl 4-hydroxy-1-piperidinecarboxylate
- Purity
- 97%
- Packaging
- 10ml
- Price
- $174
- Updated
- 2023/06/20
- Product number
- B4869
- Product name
- Benzyl 4-Hydroxy-1-piperidinecarboxylate
- Purity
- >98.0%(GC)
- Packaging
- 5g
- Price
- $50
- Updated
- 2025/07/31
- Product number
- B4869
- Product name
- Benzyl 4-Hydroxy-1-piperidinecarboxylate
- Purity
- >98.0%(GC)
- Packaging
- 25g
- Price
- $161
- Updated
- 2025/07/31
- Product number
- B130108
- Product name
- Benzyl4-Hydroxypiperidine-1-carboxylate
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- FB44151
- Product name
- Benzyl 4-hydroxy-1-piperidinecarboxylate
- Packaging
- 500g
- Price
- $750
- Updated
- 2021/12/16
Benzyl 4-hydroxy-1-piperidinecarboxylate Chemical Properties,Usage,Production
Uses
Reactant for synthesis of:
Orally bioavailable P2Y12 antagonists for inhibition of platelet aggregation
Piperidine derivatives
Molecular rods
Oxazolidinone-quinolone hybrids and their antibacterial activity
Cyclic prodrug of RGD peptidomimetic
Reactant for oxidation of alcohols
Synthesis
5382-16-1
501-53-1
95798-23-5
General procedure for the synthesis of N-Benzyloxycarbonyl-4-hydroxypiperidine from 4-hydroxypiperidine and benzyl chloroformate: over 30 min, benzyl chloroformate (8.55 mL; 60 mmol) was slowly added dropwise to a well-stirred 4-hydroxypiperidine (5 g; 49.44 mmol), a 1N aqueous NaOH solution (60 mL; 60 mmol) and dioxane (60 mL) in a in a cooled mixture. After dropwise addition, the reaction mixture was continued to stir for 30 minutes. Upon completion of the reaction, the reaction mixture was treated with water and subsequently concentrated and acidified with hydrochloric acid to pH 2. The acidified aqueous phase was extracted with EtOAc, the organic phases were combined, washed with water and saturated brine in that order, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The crude product was purified by fast column chromatography (silica gel was the stationary phase, and the eluents were petroleum ether with 50% dichloromethane (60-80 °C) and 10% acetonitrile containing 2% methanol in chloroform solution). The final product was 12.5 g (99% yield) of N-Cbz-4-hydroxypiperidine as an oil; mass spectrum (chemical ionization): m/z 236 (M++1), 218, 192, 174, 91.
References
[1] Patent: WO2005/35495, 2005, A2. Location in patent: Page/Page column 129
[2] Patent: US7759387, 2010, B2. Location in patent: Page/Page column 113
[3] Bioorganic Chemistry, 2002, vol. 30, # 4, p. 285 - 301
[4] Chemistry - A European Journal, 2007, vol. 13, # 17, p. 4859 - 4872
[5] Angewandte Chemie - International Edition, 2014, vol. 53, # 12, p. 3236 - 3240
Benzyl 4-hydroxy-1-piperidinecarboxylate Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from Benzyl 4-hydroxy-1-piperidinecarboxylate manufacturers
- Product
- Benzyl 4-hydroxy-1-piperidinecarboxylate 95798-23-5
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 98%
- Supply Ability
- 150KG
- Release date
- 2019-07-01