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Molecule
ID:38377
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₉NO₃
Molecular Mass
201.26276
Exact Mass
201.13649347
Charge
0
InChI
InChI=1S/C10H19NO3/c1-10(2,3)14-9(13)11-6-4-5-8(12)7-11/h8,12H,4-7H2,1-3H3
InChIKey
UIJXHKXIOCDSEB-UHFFFAOYSA-N
Canonic Smiles
OC1CCCN(C1)C(=O)OC(C)(C)C
Isomeric Smiles
C1CN(CC(C1)O)C(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
14.863168
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.86577713
LogD (pH = 7.4)
0.8657771
Log P
0.86577713
Molar Refractivity
53.192
Polarizability
20.97339
Polar Surface Area
49.77
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
•
IUPAC name
•
IUPAC Traditional name
•
Synonyms
Registration numbers
Properties
•
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
•
PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR0870
Maybridge
MO07159
Sigma Aldrich
94647
Matrix Scientific
041245
Alfa Aesar
L17600
Enamine
EN300-57281
Academic Data
PubChem
545699
Names and Identifiers
IUPAC name
tert-butyl 3-hydroxypiperidine-1-carboxylate
IUPAC Traditional name
tert-butyl 3-hydroxypiperidine-1-carboxylate
Synonyms
1-Boc-3-hydroxypiperidine
3-Hydroxypiperidine, N-BOC protected
1-(tert-Butoxycarbonyl)-3-hydroxypiperidine
tert-butyl 3-hydroxypiperidine-1-carboxylate
1-Boc-3-hydroxypiperidine
3-羟基-1-哌啶甲酸叔丁酯
1-BOC-3-羟基哌啶
N-Boc-3-哌啶醇
tert-Butyl 3-hydroxy-1-piperidinecarboxylate
1-Boc-3-piperidinol
Registration numbers
MDL Number
MFCD02093938
CAS Number
85275-45-2
EC Number
000-000-0
Beilstein Number
4180859
PubChem SID
24890035
161001684
PubChem CID
545699
Properties
Product Information
Purity
97%
Source
≥98.0% (TLC)
Source
95%
Source
Empirical Formula (Hill Notation)
C10H19NO3
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
否
Source
Safety Statements
26
-
36
Source
26
-
37
Source
German water hazard class
3
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Risk Statements
36/37/38
Source
GHS Signal Word
Warning
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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
Physical Property
Hydrophobicity(logP)
1.607
Source
Melting Point
66-70°C
Source
Molecule Details
Sigma Aldrich
94647
Packaging
1 g in poly tube
5 g in poly bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
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MDL Number
•
CAS Number
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EC Number
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Beilstein Number
•
PubChem SID
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PubChem CID