ChemicalBook >> CAS DataBase List >>4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester

4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester

CAS No.
183673-66-7
Chemical Name:
4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester
Synonyms
FMOC-PIP(BOC)-OH;1-BOC-PIPERIDINE-4-FMOC-AMINO-4-CARBOXYLIC ACID;Fmoc-L-Pip(Boc)-OH;1-BOC-4-FMOC-PIP-OH;FMOC-4,4-ACP(1-N-BOC);BOC-PIC(4)(4-NHBOC)-OH;1-N-Boc-4-N-Fmoc-Aminopiperi;1-BOC-4-N-FMOC-AMINO-PIPERIDINE;1-Boc-4-(Fmoc-amino)piperidine-4;1-N-BOC-4-N-FMOC-AMINO-4-CARBOXYLIC-PIPERIDINE
CBNumber:
CB2673000
Molecular Formula:
C26H30N2O6
Molecular Weight:
466.53
MDL Number:
MFCD01318741
MOL File:
183673-66-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:51:23

4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester Properties

Melting point 80-82 °C
Boiling point 569.36°C (rough estimate)
Density 1.2464 (rough estimate)
refractive index 1.5300 (estimate)
storage temp. Inert atmosphere,2-8°C
pka 3.80±0.20(Predicted)
Appearance White to off-white Solid
CAS DataBase Reference 183673-66-7(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
10
HS Code  29225090

4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester price More Price(67)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Usbiological 262885 N-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid 183673-66-7 250mg $446 2026-06-03 Buy
Usbiological 262885 N-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid 183673-66-7 500mg $679 2026-06-03 Buy
Usbiological 262885 N-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid 183673-66-7 1g $1044 2026-06-03 Buy
Usbiological 262885 N-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid 183673-66-7 2g $1650 2026-06-03 Buy
Usbiological 262885 N-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid 183673-66-7 5g $2696 2026-06-03 Buy
Product number Packaging Price Buy
262885 250mg $446 Buy
262885 500mg $679 Buy
262885 1g $1044 Buy
262885 2g $1650 Buy
262885 5g $2696 Buy

4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester Chemical Properties, Uses, Production

Chemical Properties

N-Boc-amino-(4-N-Fmoc-piperidinyl)carboxylic Acid is white to cream crystalline powder or chunks

Uses

N-Boc-amino-(4-N-Fmoc-piperidinyl)carboxylic acid is used in the preparation of synthetic peptide amides as kappa opioid receptor agonists for treatment of pain, pruritis and inflammation associated w ith a variety of diseases.

Uses

Cyclic ,-disubstituted amino acid for the preparation of water-soluble highly helical peptides.

Synthesis

9-Fluorenylmethyl chloroformate

28920-43-6

4-AMINO-1-BOC-PIPERIDINE-4-CARBOXYLIC ACID

183673-71-4

4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER

183673-66-7

The general procedure for the synthesis of 4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid from methyl chloroformate-9-fluorenylmethyl and 4-amino-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid was as follows: 4-amino-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid (5 g, 20.5 mmol) was dissolved in THF (300 mL), an aqueous solution of Na2CO3 (6.45 g, 61.5 mmol, 3.0 eq.) was added (64.5 mL) and cooled to 0 °C. A THF solution (30 mL) of methyl 9-fluorenyl chloroformate (5.3 g, 30.7 mmol, 1.5 eq.) was added slowly and dropwise. The reaction mixture was gradually warmed to 25 °C and stirring was continued for 12 hours. After completion of the reaction, the reaction solution was carefully acidified with 1 M HCl and the crude product was extracted three times with EtOAc. The organic layers were combined, dried with Na2SO4, concentrated and purified by combiflash column chromatography (eluent: 0 to 10% MeOH/DCM) to afford the target product 4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butyloxycarbonyl)piperidine-4-carboxylic acid (4.02 g, 42% yield). The product was confirmed by 1H NMR, 13C NMR and HRMS characterization.

References

[1] Organic Syntheses, 2005, vol. 81, p. 213 - 224
[2] Patent: WO2015/184349, 2015, A2. Location in patent: Paragraph 0225-0226

4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester Preparation Products And Raw materials

Global Suppliers ( 181)
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J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
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View Latest Price from 4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4-(9H-fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester pictures 2026-08-08 4-(9H-fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester
183673-66-7
$31.00-85.00 99.90% 10g TargetMol Chemicals Inc.
4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER pictures 2020-01-05 4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER
183673-66-7
$7.00 1KG 99% 100KG Career Henan Chemical Co

4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester Spectrum

1-(TERT-BUTOXYCARBONYL)-4-([(9H-FLUOREN-9-YLMETHOXY)CARBONYL]AMINO)PIPERIDINE-4-CARBOXYLIC ACID 1-(TERT-BUTOXYCARBONYL)-4-FLUORENYLMETHOXYCARBONYLAMINOPIPERIDINE-4-CARBOXYLIC ACID 1-N-BOC-4-N-FMOC-AMINO-4-CARBOXYLIC-PIPERIDINE 1-N-BOC-4-N-FMOC-AMINOPIPERIDINE-4-CARBOXYLIC ACID 1-BOC-4-FMOC-PIP-OH 1-BOC-4-(FMOC-AMINO)-PIPERIDINE-4-CARBOXYLIC ACID 4-(FMOC-AMINO)-1-BOC-PIPERIDINE-4-CARBOXYLIC ACID 4-[[(9H-Fluoren-9-ylMethoxy)carbonyl]aMino]-1,4-piperidinedicarboxylic Acid 1-(1,1-DiMethylethyl) Ester 1-BOC-4-N-FMOC-AMINO-PIPERIDINE 1-Boc-4-(FMoc-aMino)-4-piperidinecarboxylic acid BOC-PIC(4)(4-NHBOC)-OH FMOC-4,4-ACP(1-N-BOC) FMOC-4-AMINO-1-BOC-PIPERIDINE-4-CARBOXYLIC ACID N-ALPHA,GAMMA-DI-T-BUTOXYCARBONYL-4-AMINO-4-PIPECOLIC ACID N-BOC-4-N-FMOC-AMINO-4-PIPERIDINYLCARBOXYLIC ACID N-BOC-4-(FMOC-AMINO)PIPERIDINE-4-CARBOXYLIC ACID N-(9-FLUORENYLMETHOXYCARBONYL)-AMINO-(4-N-(TERT-BUTOXYCARBONYL)-PIPERIDINYL)CARBOXYLIC ACID 1-[(tert-butoxy)carbonyl]-4-[(9H-fluoren-9-ylMethoxy)carbonyl]piperidine-4-carboxylic acid 1-(tert-butoxycarbonyl)-4-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-piperidinecarboxylic acid N-FMOC-AMINO-(4-N-BOC-PIPERIDINYL) CARBOXYLIC ACID 4-(((9H-fluoren-9-yl)Methoxy)carbonylaMino)-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid 4-(((9H-Fluoren-9-yl)methoxy)carbonylamino)-1-(tert-butoxycarbonyl)piperidine-4-carboxylic aci 1-Boc-piperidine-4-Fmoc-amino-4-carboxylic acid≥ 97% (HPLC) Fmoc-L-Pip(Boc)-OH 1-Boc-4-(N-Fmoc-amino)piperidine-4-carboxylic acid 1,4-Piperidinedicarboxylicacid,4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,1-(1,1-dimethylethyl)ester(9CI) 1-Boc-piperidine-4-N-Fmoc-amino-4-carboxylicacid N-FMOC-Amino-(4-N-BOC-piperidinyl)carboxylicacid,95% 1-N-Boc-4-N-Fmoc-Aminopiperi 4-N-Fmoc-amino-1-N-Bocpiperidine-4-carboxylic acid 1-(N-Boc)-4-(Fmoc-amino)-piperidine-4-carboxylic acid 4-(((9H-fluoren-9-yl)methoxy)carbonyl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid 4-(9H-fluoren-9-ylmethoxycarbonylamino)-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-4-carboxylicaci 4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER USP/EP/BP 4-(9H-fluoren-9-ylmethoxycarbonylamino)-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-4-carboxylic acid 1-Boc-4-(Fmoc-amino)piperidine-4 1-(1,1-Dimethylethyl) 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-1,4-piperidinedicarboxylate 1-Boc-Pi'ceridine-4-Fmoc-amino-4-carboxylic acid 4-(9H-fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester, 10 mM in DMSO 1-BOC-PIPERIDINE-4-FMOC-AMINO-4-CARBOXYLIC ACID FMOC-PIP(BOC)-OH 4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester 183673-66-7 83673-66-7 C26H30N2O6 Peptide Synthesis Specialty Synthesis Unnatural Amino Acid Derivatives Others Heterocycles Others Peptide Synthesis Unnatural Amino Acid Derivatives FMOC amino acids Amino Acid Derivatives Amino Acids & Derivatives