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Molecule
ID:33075
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₂₀N₂O₂
Molecular Mass
200.278
Exact Mass
200.15247789
Charge
0
InChI
InChI=1S/C10H20N2O2/c1-10(2,3)14-9(13)12-8-4-6-11-7-5-8/h8,11H,4-7H2,1-3H3,(H,12,13)
InChIKey
CKXZPVPIDOJLLM-UHFFFAOYSA-N
Canonic Smiles
O=C(OC(C)(C)C)NC1CCNCC1
Isomeric Smiles
C(=O)(NC1CCNCC1)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
15.293134
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
-2.7098007
LogD (pH = 7.4)
-2.0254052
Log P
0.5103967
Molar Refractivity
54.9482
Polarizability
21.854008
Polar Surface Area
50.36
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
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PubChem SID
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PubChem CID
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MDL Number
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CAS Number
Properties
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Product Information
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Safety Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
035820
Apollo Scientific
OR0807
Key Organics
6X-5030
InterBioScreen
BB_SC-4784
Sigma Aldrich
540935
Chemik
CHH15556
Enamine
EN300-36333
Bide Pharmatech
BD0339
Alfa Aesar
H28517
Academic Data
PubChem
723833
Names and Identifiers
Synonyms
tert-Butyl piperidin-4-ylcarbamate
4-(Boc-amino)-piperidine
4-Aminopiperidine, 4-BOC protected
tert-Butyl piperidin-4-ylcarbamate
4-(N-Boc-amino)piperidine
4-(N-Boc-氨基)哌啶
tert-butyl N-(4-piperidinyl)carbamate
4-(Boc-amino)piperidine
4-Boc-氨基哌啶
4-(N-Boc-amino)piperidine
IUPAC Traditional name
tert-butyl N-(piperidin-4-yl)carbamate
IUPAC name
tert-butyl N-(piperidin-4-yl)carbamate
Registration numbers
PubChem SID
160996382
24878503
PubChem CID
723833
MDL Number
MFCD00798171
CAS Number
73874-95-0
Properties
Product Information
Purity
97%
Source
>95%
Source
96%
Source
95%
Source
Empirical Formula (Hill Notation)
C10H20N2O2
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
Harmful/Keep Cold
Source
Air Sensitive
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Signal Word
Warning
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
European Hazard Symbols
Irritant (Xi)
Source
German water hazard class
3
Source
Safety Statements
26
-
36
Source
26
-
37
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Risk Statements
36/37/38
Source
Physical Property
Melting Point
155-160°C
Source
162-166 °C(lit.)
Source
159 - 161°C
Source
162-166°C
Source
Hydrophobicity(logP)
0.691
Source
Molecule Details
Sigma Aldrich
540935
Application
Pharma building block.1
Used in a synthesis of a piperidine-4-carboxamide CCR5 antagonist with potent anti-HIV-1 activity.
Packaging
1, 5, 25 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay