ChemicalBook >> CAS DataBase List >>Ethyl 1-Boc-3-piperidinecarboxylate

Ethyl 1-Boc-3-piperidinecarboxylate

CAS No.
130250-54-3
Chemical Name:
Ethyl 1-Boc-3-piperidinecarboxylate
Synonyms
BOC-DL-NIPC-OET;BOC-DL-PIC(3)-OET;BOC-DL-PIC(3)-EOT;ETHYL N-BOC-NIPECOTATE;1-BOC-ETHYL NIPECOTATE;Ethyl 1-Boc-nipecotate;N-BOC S-ethyl nipecotate;Ethyl N-Boc-DL-nipecotate;1-Boc-3-piperidinecarboxyL;BOC-DLChemicalbook-PIC(3)-EOT
CBNumber:
CB9454527
Molecular Formula:
C13H23NO4
Molecular Weight:
257.33
MDL Number:
MFCD04116274
MOL File:
130250-54-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 04:57:46

Ethyl 1-Boc-3-piperidinecarboxylate Properties

Melting point 31-35℃
Boiling point 95℃/0.5mm
Density 1.077±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka -2.40±0.40(Predicted)
form powder to lump
color White to Yellow to Orange
Sensitive Moisture & Light Sensitive
BRN 3614917
InChI InChI=1S/C13H23NO4/c1-5-17-11(15)10-7-6-8-14(9-10)12(16)18-13(2,3)4/h10H,5-9H2,1-4H3
InChIKey YCXCRFGBFZTUSU-UHFFFAOYSA-N
SMILES N1(C(OC(C)(C)C)=O)CCCC(C(OCC)=O)C1
CAS DataBase Reference 130250-54-3(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H317-H319
Precautionary statements  P280-P301+P312+P330-P302+P352-P305+P351+P338
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xn
Risk Statements  22-36-43-52
Safety Statements  26
WGK Germany  3
HazardClass  IRRITANT
HS Code  29333990
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Eye Irrit. 2
Skin Sens. 1
NFPA 704
1
2 0

Ethyl 1-Boc-3-piperidinecarboxylate price More Price(48)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical E0954 Ethyl 1-(tert-Butoxycarbonyl)-3-piperidinecarboxylate >98.0%(GC) 130250-54-3 5g $32 2026-04-30 Buy
TCI Chemical E0954 Ethyl 1-(tert-Butoxycarbonyl)-3-piperidinecarboxylate >98.0%(GC) 130250-54-3 25g $92 2026-04-30 Buy
Apolloscientific OR309162 Ethyl piperidine-3-carboxylate, N-BOC protected >98% 130250-54-3 25g $21 2026-06-04 Buy
Apolloscientific OR309162 Ethyl piperidine-3-carboxylate, N-BOC protected >98% 130250-54-3 100g $28 2026-06-04 Buy
Apolloscientific OR309162 Ethyl piperidine-3-carboxylate, N-BOC protected >98% 130250-54-3 500g $131 2026-06-04 Buy
Product number Packaging Price Buy
E0954 5g $32 Buy
E0954 25g $92 Buy
OR309162 25g $21 Buy
OR309162 100g $28 Buy
OR309162 500g $131 Buy

Ethyl 1-Boc-3-piperidinecarboxylate Chemical Properties, Uses, Production

Synthesis

Boc₂O (7.75 mL, 33.4 mmol) was added to a solution of ethyl piperidine-3-carboxylate (15 g, 95 mmol) in THF (159 mL) at room temperature, and the mixture was stirred for 16 h at room temperature. The resulting reaction mass was diluted with water (50 mL) and then extracted with ethyl acetate (3 x 100 mL). The combined organic extract was washed with saturated NaHCO₃ solution (1 x 200 mL) and brine (20 mL), dried (Na₂SO₄), filtered, and concentrated. The resulting residue was purified by ELSD ISCO on a 120 g silica gel column, eluting the compound in hexane to approximately 25% ethyl acetate. The pure fraction was collected and concentrated to give the desired product, 1-tert-butyl-3-ethylpiperidine-1,3-dicarboxylate. The final product, ethyl Ethyl 1-Boc-3-piperidinecarboxylate, was obtained in a yield of 23.39 g, 91 mmol, 95%.

Synthetic Route of Ethyl 1-Boc-3-piperidinecarboxylate

Chemical Properties

White powder

Uses

Reactant for synthesis of:

  • GABAA receptor agonists
  • Piperidine derivatives
  • Selective TACE inhibitors
  • HDL-elevating agents
  • α-Sulfonyl hydroxamic acid derivatives
  • chemicals in the Iboga-alkaloid family

Uses

Reactant for synthesis of:• ;GABAA receptor agonists1• ;Piperidine derivatives2• ;Selective TACE inhibitors3• ;HDL-elevating agents4• ;α-Sulfonyl hydroxamic acid derivatives5• ;chemicals in the Iboga-alkaloid family6

Ethyl 1-Boc-3-piperidinecarboxylate Preparation Products And Raw materials

Global Suppliers ( 246)
Supplier Tel Email Country ProdList Advantage
Shanghai Hobor Chemical Co., Ltd 13918007836 sales@hoborchem.com China 423 60
Anhui Dexinjia Biopharm Co., Ltd 0531-82375893 15553111391 phoebe@jndxj.com China 285 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Chembest Research Laboratories Limited 021-20908456 sales@BioChemBest.com China 5996 61
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Shijiazhuang Sdyano Fine Chemical Co., Ltd. 0311-89250318 13582355795 master@sjzsdyn.com China 2776 65
Wuhan Chemwish Technology Co., Ltd 86-027-67849912 sales@chemwish.com China 35884 56

View Latest Price from Ethyl 1-Boc-3-piperidinecarboxylate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ethyl 1-Boc-3-piperidinecarboxylate pictures 2024-04-02 Ethyl 1-Boc-3-piperidinecarboxylate
130250-54-3
$10.00-100.00 1kg 99% 5000 Metric Ton/Month Wuhan Xinhao Biotechnology Co., Ltd
Ethyl 1-Boc-3-piperidinecarboxylate pictures 2023-11-03 Ethyl 1-Boc-3-piperidinecarboxylate
130250-54-3
$10.00 1kg 99% 100tons Anhui Zhongda Biotechnology Co., Ltd
Ethyl 1-Boc-3-piperidinecarboxylate pictures 2023-06-26 Ethyl 1-Boc-3-piperidinecarboxylate
130250-54-3
$150.00 10g 99% 500kg/month Hebei Mingeng Biotechnology Co., Ltd

Ethyl 1-Boc-3-piperidinecarboxylate Spectrum

1-(TERT-BUTOXYCARBONYL)-3-(ETHOXYCARBONYL)PIPERIDINE ETHYL 1-BOC-3-PIPERIDINECARBOXYLATE ETHYL N-BOC-NIPECOTATE BOC-DL-NIPC-OET BOC-DL-PIC(3)-EOT BOC-DL-PIC(3)-OET N-T-BUTOXYCARBONYL-DL-NIPECOTIC ACID ETHYL ESTER N-T-BUTOXYCARBONYL-DL-PIPERIDINECARBOXYLIC ACID ETHYL ESTER N-T-BUTOXYCARBONYL-DL-3-PIPERIDINECARBOXYLIC ACID ETHYL ESTER N-T-BUTOXYCARBONYL-(R,S)-PIPERIDINE-3-CARBOXYLIC ACID ETHYL ESTER N-T-BUTOXYCARBONYL-(R,S)-NIPECOTIC ACID ETHYL ESTER N-T-BUTOXYCARBONYL-(R,S)-NIPOCITUC ACID ETHYL ESTER N-T-BUTOXYCARBONYL-(+/-)-NIPECOTIC ACID ESTER N-T-BUTOXYCARBONYL-(+/-)-NIPECOTIC ACID ETHYL ESTER PIPERIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER 3-ETHYL ESTER 1-Boc-3-Piperidinecarboxylic acid ethyl ester 1-BOC-ETHYL NIPECOTATE 1,3-Piperidinedicarboxylic acid, 1-(1,1-dimethylethyl) 3-ethyl ester 1-(tert-butyl) 3-ethyl tetrahydro-1,3(2H)-pyridinedicarboxylate 1-(tert-Butyl) 3-ethyl 1,3-piperidinedicarboxylate 1-Boc-3-piperidinecarboxylate ethyl ester 1-Boc-piperidine-3-carboxylic acid ethyl ester N-Boc-3-piperidinecarboxylate ethyl ester 1-(tert-Butoxycarbonyl)-piperidine-3-carboxylic acid ethyl ester Ethyl N-Boc-DL-nipecotate N-Boc-DL-nipecotic acid ethyl ester 1-tert-butyl 3-ethyl piperidine-1,3-dicarboxylate 1-Boc-nipecotic acid ethyl ester, 97% Ethyl N-Boc-3-piperidinecarboxylate Ethyl 1-(tert-Butoxycarbonyl)-3-piperidinecarboxylate N-Boc-Piperidine-3-carboxylate or ethyl 1-Boc-piperidine-3-carboxylate N-Boc-piperidine-3-carboxylic acid ethyl ester Piperidine-1,3-dicarboxylic acid 1-tert-butyl 3-ethyl ester Ethyl 1-Boc-DL-nipecotate, 97% N-BOC-3-piperidine forMic acid ethyl ester 1-Boc-piperidine-3-carboxylic acid ethyl eater Piperidine derivative CAS NO.130250-54-3 Ethyl-N-BOC-piperidine-3-carboxylate Piperidine derivative Ethyl-N-BOC-piperidine-3-carboxylate Ethyl1-(tert-Butoxycarbonyl)-3-piperidinecarboxylate> N-BOC S-ethyl nipecotate 1-Boc-3-piperidinecarboxyL N-Boc-piperidine-3-carboxylate, ethyl ester 1-(tert-Butoxycarbonyl)-3-piperidinecarboxylic Acid Ethyl Ester 1-(tert-Butoxycarbonyl)nipecotic Acid Ethyl Es Ethyl 1-(tert-Butoxycarbonyl)nipecotate Ethyl 1-Boc-nipecotate BOC-DLChemicalbook-PIC(3)-EOT Piperidine-1,3-dicarboxylic acid 1-tert-butyl 3-ethyl Ethyl N-Boc-piperidine-3-carboxylate N-Boc-3-piperidinecarboxylic acid ethyl ester Ethyl piperidine-3-carboxylate, N-BOC protected 1-tert-Butyl 3-ethyl piperidin-1,3-dicarboxylate 130250-54-3 Building Blocks C13 Chemical Synthesis Heterocyclic Building Blocks Piperidines