ChemicalBook >> CAS DataBase List >>Benzyl 4-hydroxy-1-piperidinecarboxylate

Benzyl 4-hydroxy-1-piperidinecarboxylate

CAS No.
95798-23-5
Chemical Name:
Benzyl 4-hydroxy-1-piperidinecarboxylate
Synonyms
BENZYL 4-HYDROXYPIPERIDINE-1-CARBOXYLATE;1-Cbz-4-hydroxypiperidine;N-CBZ-4-HYDROXY-1-PIPERIDINE;BUTTPARK 93\50-53;1-Cbz-4-piperidinol;1-CBZ-4-hydroxypethidine;N-CBZ-4-HYDROXYPIPERIDINE;1-Carbobenzoxy-4-piperidinol;1-Carbobenzoxy-4-hydroxypiperidine;1-(Benzyloxycarbonyl)-4-piperidinol
CBNumber:
CB5199534
Molecular Formula:
C13H17NO3
Molecular Weight:
235.28
MDL Number:
MFCD01863722
MOL File:
95798-23-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 03:55:09
Product description Number Pack Size Price
Benzyl 4-hydroxy-1-piperidinecarboxylate 97% 513903 10ml $174
Benzyl 4-Hydroxy-1-piperidinecarboxylate >98.0%(GC) B4869 5g $50
Benzyl 4-Hydroxy-1-piperidinecarboxylate >98.0%(GC) B4869 25g $161
Benzyl 4-hydroxy-1-piperidinecarboxylate FB44151 0.1kg $250
Benzyl 4-hydroxy-1-piperidinecarboxylate FB44151 0.25kg $354
More product size

Benzyl 4-hydroxy-1-piperidinecarboxylate Properties

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)
UNSPSC Code 12352100

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
Hazard Note  Irritant
HS Code  2933399990

Benzyl 4-hydroxy-1-piperidinecarboxylate price More Price(62)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 513903 Benzyl 4-hydroxy-1-piperidinecarboxylate 97% 95798-23-5 10ml $174 2023-06-20 Buy
TCI Chemical B4869 Benzyl 4-Hydroxy-1-piperidinecarboxylate >98.0%(GC) 95798-23-5 5g $50 2026-04-30 Buy
TCI Chemical B4869 Benzyl 4-Hydroxy-1-piperidinecarboxylate >98.0%(GC) 95798-23-5 25g $161 2026-04-30 Buy
Biosynth FB44151 Benzyl 4-hydroxy-1-piperidinecarboxylate 95798-23-5 0.1kg $250 2026-06-04 Buy
Biosynth FB44151 Benzyl 4-hydroxy-1-piperidinecarboxylate 95798-23-5 0.25kg $354 2026-06-04 Buy
Product number Packaging Price Buy
513903 10ml $174 Buy
B4869 5g $50 Buy
B4869 25g $161 Buy
FB44151 0.1kg $250 Buy
FB44151 0.25kg $354 Buy

Benzyl 4-hydroxy-1-piperidinecarboxylate Chemical Properties,Uses,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

4-Hydroxypiperidine

5382-16-1

Benzyl chloroformate

501-53-1

Benzyl 4-hydroxy-1-piperidinecarboxylate

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

19099-93-5
95798-23-5
Synthesis of Benzyl 4-hydroxy-1-piperidinecarboxylate from 1-Cbz-4-Piperidone
Global( 127)Suppliers
Supplier Tel Email Country ProdList Advantage
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29815 58
Jinan Carbotang Biotech Co.,Ltd.
+8615866703830 figo.gao@foxmail.com China 8497 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49979 58
Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
+8613580539051 joe@yuhengpharm.com CHINA 21142 58
Hefei Hirisun Pharmatech Co., Ltd
+8615056975894 shawn@hirisunpharm.com CHINA 9911 58
CD Chemical Group Limited
+8615986615575 info@codchem.com China 17259 58
Labnetwork lnc.
+86-27-50766799 +8618062016861 contact@labnetwork.com China 19987 58
PT CHEM GROUP LIMITED
+86-85511178; peter68@ptchemgroup.com China 35425 58
Sichuan Biosynce Pharmatech Co., Ltd.
+8619950309693 diane@biosynce.com China 4871 58

View Lastest Price from Benzyl 4-hydroxy-1-piperidinecarboxylate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Benzyl 4-hydroxy-1-piperidinecarboxylate pictures 2019-07-06 Benzyl 4-hydroxy-1-piperidinecarboxylate
95798-23-5
$1.00 1KG 98% 150KG Career Henan Chemical Co
4-hydroxy-2-piperidinecarboxylic acid (phenylmethyl) ester BENZYL 4-HYDROXY-1-PIPERIDINECARBOXYLATE BENZYL 4-HYDROXYTETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE BUTTPARK 93\50-53 N-Benzyloxycarbonyl-4-Hydroxypiperidine 4-HYDROXY-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER 4-HYDROXYPIPERIDINE, N-CBZ PROTECTED 4-Hydroxypiperidine, N-CBZ protected 97% N-CBZ-4-HYDROXYPIPERIDINE Benzyl 4-hydroxy-1-piperidinecarboxylate 97% 1-CBZ-4-hydroxypethidine 1-(Benzyloxycarbonyl)-4-piperidinol 1-(benzyloxycarbonyl)-4-hydroxypiperidine Benzyl 4-Hydroxy-1-piperidinecarboxylate > 1-Piperidinecarboxylic acid, 4-hydroxy-, phenylmethyl ester 1-Carbobenzoxy-4-hydroxypiperidine 1-Carbobenzoxy-4-piperidinol 1-Cbz-4-piperidinol 4-Hydroxy-1-piperidinecarboxylic Acid Benzyl Ester 1-Cbz-4-hydroxypiperidine BENZYL 4-HYDROXYPIPERIDINE-1-CARBOXYLATE N-CBZ-4-HYDROXY-1-PIPERIDINE 95798-23-5 Building Blocks Piperidines Heterocyclic Building Blocks API intermediates Building Blocks Heterocyclic Building Blocks Piperidines pharmacetical