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Molecule
ID:30519
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)13-7-5-4-6-9(13)8-12/h9H,4-8,12H2,1-3H3
InChIKey
PTVRCUVHYMGECC-UHFFFAOYSA-N
Canonic Smiles
NCC1CCCCN1C(=O)OC(C)(C)C
Isomeric Smiles
C(=O)(N1C(CN)CCCC1)OC(C)(C)C
Calculated Properties
JChem
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
-1.7403206
LogD (pH = 7.4)
-0.5544711
Log P
1.203464
Molar Refractivity
59.4505
Polarizability
23.692034
Polar Surface Area
55.56
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
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
IUPAC name
•
IUPAC Traditional name
•
Synonyms
Registration numbers
•
MDL Number
•
CAS Number
•
PubChem SID
•
PubChem CID
Properties
•
Safety Information
•
Product Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
033175
Sigma Aldrich
687154
Chemik
CHH15700
Enamine
EN300-56414
Bide Pharmatech
BD0669
Alfa Aesar
H54507
A&J Pharmtech
AJA-O17386
Academic Data
PubChem
2756482
Names and Identifiers
IUPAC name
tert-butyl 2-(aminomethyl)piperidine-1-carboxylate
IUPAC Traditional name
tert-butyl 2-(aminomethyl)piperidine-1-carboxylate
Synonyms
2-Aminomethyl-piperidine-1-carboxylic acid tert-butyl ester
2-(Aminomethyl)-1-N-Boc-piperidine
2-Aminomethyl-1-Boc-piperidine
1-Boc-(2-Aminomethyl)piperidine
1,1-Dimethylethyl 2-(aminomethyl)-1-piperidinecarboxylate
1-Boc-2-aminomethylpiperidine
1-Boc-2-氨甲基哌啶
2-Aminomethylpiperidine-1-carboxylic acid tert-butyl ester
tert-butyl 2-(aminomethyl)piperidine-1-carboxylate
Registration numbers
MDL Number
MFCD01317791
CAS Number
177911-87-4
370069-31-1
PubChem SID
160993826
PubChem CID
2756482
Molecule Details
Sigma Aldrich
687154
Packaging
1 g in glass bottle
Application
Reactant for synthesis of:
• TRPV1 antagonists1
• CHK1 inhibitors2
• p38a MAP kinase inhibitors3
• Carbamoylphosphonates4
• Macrolactams via carbonylation/intramolecular amidation5
• Intramolecular transamidation6
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Safety Statements
26
-
61
Source
23
-
26
-
36/37
-
57
-
60
Source
German water hazard class
3
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H302
-
H315
-
H319
-
H335
-
H400
Source
H301
-
H315
-
H319
-
H335
-
H400
Source
Hazard Class
9
Source
GHS Pictograms
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
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
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
UN Number
3082
Source
UN3082
Source
European Hazard Symbols
Harmful (Xn)
Source
Nature polluting (N)
Harmful (X)
RID/ADR
UN 3082 9/PG 3
Source
Risk Statements
22
-
36/37/38
-
50
Source
Packing Group
3
Source
III
Source
Personal Protective Equipment
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
GHS Precautionary statements
P261
-
P273
-
P305+P351+P338
Source
P261
-
P301+P310
-
P305+P351+P338
-
P302+P352
-
P405
-P501A
Source
Product Information
Empirical Formula (Hill Notation)
C11H22N2O2
Source
Purity
95%
Source
95+%
Source
97%
Source
Physical Property
Refractive Index
n20/D 1.4745
Source
1.4745
Source
Flash Point
>230 °F
Source
>110 °C
Source
>110°C(230°F)
Source
Density
1.0124 g/mL at 25 °C
Source
1.012
Source
2.303
Source
Source
Source
Source
Source
Hydrophobicity(logP)