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Molecule
ID:15769
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₂₂N₂O₂
Molecular Mass
214.30458
Exact Mass
214.16812795
Charge
0
InChI
InChI=1S/C11H22N2O2/c1-11(2,3)15-10(14)13-8-9-5-4-6-12-7-9/h9,12H,4-8H2,1-3H3,(H,13,14)
InChIKey
KHPQHXGYYXYTDN-UHFFFAOYSA-N
Canonic Smiles
O=C(OC(C)(C)C)NCC1CCCNC1
Isomeric Smiles
N1CC(CCC1)CNC(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
15.843377
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
-2.215348
LogD (pH = 7.4)
-1.670643
Log P
1.0125542
Molar Refractivity
59.6674
Polarizability
23.692034
Polar Surface Area
50.36
Rotatable Bonds
4
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
Data Source
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Academic Data
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IUPAC Traditional name
•
IUPAC name
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Synonyms
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Safety Information
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Physical Property
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Product Information
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
016374
Apollo Scientific
OR5910
ChemBridge
4036732
Sigma Aldrich
653896
55787
Chemik
CHH19005
Enamine
EN300-55508
Bide Pharmatech
BD0671
Alfa Aesar
H60257
Academic Data
PubChem
2756030
Names and Identifiers
IUPAC Traditional name
tert-butyl N-(piperidin-3-ylmethyl)carbamate
IUPAC name
tert-butyl N-(piperidin-3-ylmethyl)carbamate
Synonyms
tert-Butyl (piperidin-3-ylmethyl)carbamate
3-(Aminomethyl)piperidine, 3-BOC protected
tert-Butyl (piperidin-3-ylmethyl)carbamate
3-(Boc-氨基甲基)哌啶
(Piperidin-3-ylmethyl) carbamic acid tert-butyl ester
3-叔丁氧羰基氨甲基哌啶
tert-Butyl (piperidin-3-ylmethyl) carbamate
(3-Piperidinylmethyl)-carbamic acid 1,1-dimethylethyl ester
3-(Boc-aminomethyl)piperidine
N-(3-哌啶基甲基)氨基甲酸叔丁酯
(±)-3-(Boc-氨基甲基)哌啶
tert-Butyl N-(3-piperidylmethyl)carbamate
(±)-3-(Boc-aminomethyl)piperidine
2,6-Dimethoxy naphthalene
tert-butyl N-(piperidin-3-ylmethyl)carbamate
3-(tert-Butoxycarbonylaminomethyl)piperidine
3-Boc-Aminomethylpiperidine
Registration numbers
PubChem SID
160979076
24883999
24879700
PubChem CID
2756030
MDL Number
MFCD01632454
CAS Number
142643-29-6
Beilstein Number
7023643
EC Number
201-273-0
Molecule Details
Sigma Aldrich
653896
Packaging
1, 10 g in glass bottle
Application
Reagent for:
• Preparation of 9-substituted phenanthrene-based tylophorine analogs1
• Enzymatic acylation2
55787
Packaging
500 mg in poly tube
Application
Reagent for: Preparation of Tylophorine analogs1 Enzymatic acylation2
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
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PubChem SID
•
PubChem CID
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MDL Number
•
CAS Number
•
Beilstein Number
•
EC Number
Properties
Safety Information
Storage Warning
IRRITANT
Source
Corrosive/Keep Cold
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
3
Source
UN 3259 8/PG 2
Source
34
Source
P280
-
P305+P351+P338
-
P310
Source
P260
-
P303+P361+P353
-
P305+P351+P338
-
P301+P330+P331
-
P405
-
P501
8
Source
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
Source
Danger
Source
26
-
36/37/39
-
45
Source
4
-
9
-
20
-
28
-
36/37
-
45
-
60
3259
Source
UN3259
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
H314
Source
H314
-
H318
Source
Corrosive (C)
2
Source
II
Source
2-8°C
Source
Physical Property
60-70°C
Source
60-70 °C(lit.)
Source
60-70°C
Source
1.31
Source
Product Information
C5H10NCH2NHCO2C4H9
Source
95%
Source
≥98.0% (TLC)
Source
95+%
Source
98%
Source
C11H22N2O2
Source
Source
Source
Source
Source
German water hazard class
RID/ADR
Risk Statements
GHS Precautionary statements
Hazard Class
Personal Protective Equipment
GHS Signal Word
Safety Statements
UN Number
GHS Pictograms
GHS Hazard statements
European Hazard Symbols
Packing Group
Storage Temperature
Melting Point
Hydrophobicity(logP)
Linear Formula
Purity
Empirical Formula (Hill Notation)