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Molecule
ID:15045
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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)12-6-4-8(11)5-7-12/h8H,4-7,11H2,1-3H3
InChIKey
LZRDHSFPLUWYAX-UHFFFAOYSA-N
Canonic Smiles
NC1CCN(CC1)C(=O)OC(C)(C)C
Isomeric Smiles
N1(CCC(CC1)N)C(=O)OC(C)(C)C
Calculated Properties
JChem
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
-2.7163312
LogD (pH = 7.4)
-2.1473374
Log P
0.3014924
Molar Refractivity
55.0703
Polarizability
21.854008
Polar Surface Area
55.56
Rotatable Bonds
2
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
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC Traditional name
•
IUPAC name
Registration numbers
•
MDL Number
•
CAS Number
•
PubChem SID
•
PubChem CID
Properties
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Physical Property
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Safety Information
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
•
PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
4003509
Matrix Scientific
012595
Apollo Scientific
OR9845
Sigma Aldrich
640042
69001
Chemik
FDC07011
Enamine
EN300-39611
Bide Pharmatech
BD0337
Alfa Aesar
H30779
A&J Pharmtech
AJA-O17378
Academic Data
PubChem
1268291
Names and Identifiers
Synonyms
tert-butyl 4-aminopiperidine-1-carboxylate
1-N-BOC-4-aminopiperidine
1-Boc-4-氨基哌啶
4-Amino-1-Boc-piperidine
1-Boc-4-piperidinamine
4-氨基-1-哌啶甲酸叔丁酯
tert-Butyl 4-amino-1-piperidinecarboxylate
1-叔丁氧羰基-4-氨基哌啶
tert-Butyl 4-aminopiperidine-1-carboxylate
4-Amino-1-(tert-butoxycarbonyl)piperidine
4-Aminopiperidine, N1-BOC protected 97%
4-Amino-piperidine-1-carboxylic acid tert-butyl ester
1-Boc-4-Aminopiperidine
N-Boc-4-Aminopiperidine
1-Boc-4-氨基哌啶
IUPAC Traditional name
tert-butyl 4-aminopiperidine-1-carboxylate
IUPAC name
tert-butyl 4-aminopiperidine-1-carboxylate
Registration numbers
MDL Number
MFCD01076201
CAS Number
87120-72-7
PubChem SID
24885868
24883073
160978352
PubChem CID
1268291
Molecule Details
Sigma Aldrich
640042
Application
Employed in a microwave-assisted solid-phase synthesis of N-substituted piperidines via direct annulation of primary amines with resin-bound dimesylates.1
Packaging
1, 5 g in glass bottle
69001
Analysis Note
may contain ~5% water
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
44-48°C
Source
44-48°C
Source
Boiling Point
80°C/0.05mm
Source
80°C/0.037mm
Source
Hydrophobicity(logP)
0.881
Source
Safety Information
Storage Warning
AIR SENSITIVE, CORROSIVE
Source
Corrosive/Harmful/Air Sensitive/Store under Argon/Keep Cold
Source
Air Sensitive
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Safety Statements
26
-
36/37/39
Source
26
-
36/37/39
-
45
Source
GHS Signal Word
Danger
Source
GHS Hazard statements
H302
-
H315
-
H318
-
H335
Source
H314
-
H318
Source
Risk Statements
22
-
37/38
-
41
Source
34
Source
European Hazard Symbols
Harmful (Xn)
Source
Corrosive (C)
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Source
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Source
GHS Precautionary statements
P261
-
P280
-
P305+P351+P338
Source
P280
-
P305+P351+P338
-
P309
-
P310
Source
German water hazard class
2
Source
UN Number
UN3259
Source
Hazard Class
8
Source
Packing Group
III
Source
Product Information
Purity
98%
Source
97%
Source
≥97.0% (TLC)
Source
95%
Source
96%
Source
Empirical Formula (Hill Notation)
C10H20N2O2
Source
Grade
purum
Source
Source
Source