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

Product Name
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;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;1-BOC-PIPERIDINE-4-FMOC-AMINO-4-CARBOXYLIC ACID
CBNumber
CB2673000
Molecular Formula
C26H30N2O6
Formula Weight
466.53
MOL File
183673-66-7.mol
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4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER Property

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)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
F 
10
HS Code 
29225090
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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.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
B619250
Product name
N-Boc-amino-(4-N-Fmoc-piperidinyl)carboxylicAcid
Packaging
250mg
Price
$70
Updated
2021/12/16
Apolloscientific
Product number
OR953106
Product name
1-Boc-4-(Fmoc-amino)-4-piperidinecarboxylicacid
Purity
97%
Packaging
500mg
Price
$110
Updated
2021/12/16
Apolloscientific
Product number
OR953106
Product name
1-Boc-4-(Fmoc-amino)-4-piperidinecarboxylicacid
Purity
97%
Packaging
1g
Price
$176
Updated
2021/12/16
AK Scientific
Product number
V1376
Product name
N-Fmoc-Amino-(4-N-Boc-piperidinyl)carboxylicacid
Packaging
1g
Price
$178
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB18901
Product name
N-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid
Packaging
500mg
Price
$255
Updated
2021/12/16
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4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER Chemical Properties,Usage,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

28920-43-6

183673-71-4

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

Raw materials

Preparation Products

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View Lastest Price from 4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER manufacturers

Career Henan Chemical Co
Product
4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER 183673-66-7
Price
US $7.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100KG
Release date
2020-01-03

183673-66-7, 4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTERRelated Search:

N-BOC-ISONIPECOTIC ACID 4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER 1-Boc-4-Methylaminopiperidine FMOC-D-DAB(FMOC)-OH 1-Amino-1-cyclohexanecarboxylic acid FMOC-DAB(BOC)-OH 1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde tert-Butyl N-(3-aminopropyl)-N-methylcarbamate N-Boc-4-piperidinemethanol Ethyl 4-hydroxypiperidine-1-carboxylate 4-Amino-1-Boc-piperidine 1-Boc-piperidine 1-BOC-4-METHYLPIPERIDINE Isopropyl 4-aminopiperidine-1-carboxylate FMOC-D-DAB-OH FMOC-DAB-OH HCL Propamocarb Fmoc-Aib-OH

  • 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
  • 1-BOC-PIPERIDINE-4-FMOC-AMINO-4-CARBOXYLIC ACID
  • 4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER
  • 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
  • FMOC-PIP(BOC)-OH
  • 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
  • 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