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ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >FMOC-amino acid >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

4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER Structure
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
Molecular Weight:
466.53
MOL File:
183673-66-7.mol
MSDS File:
SDS
Modify Date:
2023/9/4 15:51:00
Request For Quotation

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)
CAS DataBase Reference 183673-66-7(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
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
F  10
HS Code  29225090

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.

4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER Preparation Products And Raw materials

Raw materials

Preparation Products

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

Global( 165)Suppliers
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A.J Chemicals 58
CLEARSYNTH LABS LTD. 58
Capot Chemical Co.,Ltd. 60
ATK CHEMICAL COMPANY LIMITED 60
Accela ChemBio Inc. 58
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career henan chemical co 58
Dideu Industries Group Limited 58
BOC Sciences 58
Dayang Chem (Hangzhou) Co.,Ltd. 58

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

4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER(183673-66-7)1HNMR

183673-66-7(4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER)Related 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
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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 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 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 1-(tert-butoxycarbonyl)-4-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-piperidinecarboxylic 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 FMOC-PIP(BOC)-OH 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 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