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Molecule
ID:39473
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₉NO₄
Molecular Mass
229.27286
Exact Mass
229.13140809
Charge
0
InChI
InChI=1S/C11H19NO4/c1-11(2,3)16-10(15)12-7-5-4-6-8(12)9(13)14/h8H,4-7H2,1-3H3,(H,13,14)/t8-/m1/s1
InChIKey
JQAOHGMPAAWWQO-MRVPVSSYSA-N
Canonic Smiles
OC(=O)[C@H]1CCCCN1C(=O)OC(C)(C)C
Isomeric Smiles
C1CN([C@H](CC1)C(=O)O)C(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
4.048332
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
0.16748306
LogD (pH = 7.4)
-1.5000744
Log P
1.6306204
Molar Refractivity
57.6604
Polarizability
22.755922
Polar Surface Area
66.84
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
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Molecule Details
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References
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Bioactivity
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General Information
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RDKit
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IUPAC Traditional name
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IUPAC name
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Related Proteins
Molecular Spectra
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Sigma Aldrich
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TRC
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR14684
Sigma Aldrich
516341
TRC
B661950
Enamine
EN300-71973
Bide Pharmatech
BD13453
Alfa Aesar
H51961
Matrix Scientific
042386
Academic Data
PubChem
688618
Names and Identifiers
IUPAC Traditional name
(2R)-1-(tert-butoxycarbonyl)piperidine-2-carboxylic acid
IUPAC name
(2R)-1-[(tert-butoxy)carbonyl]piperidine-2-carboxylic acid
Synonyms
(2S)-Piperidine-2-carboxylic acid, N-BOC protected
L-Pipecolinic acid, N-BOC protected
Boc-(R)-(+)-piperidine-2-carboxylic acid
(R)-N-Boc-piperidine-2-carboxylic acid
N-Boc-D-哌啶-2-羧酸
(R)-(+)-1-(叔丁氧羰基)-2-哌啶羧酸
(R)-(+)-1-(tert-Butoxycarbonyl)-2-piperidinecarboxylic acid
(+)-N-Boc-(R)-2-哌啶甲酸
(+)-N-Boc-(R)-pipecolinic acid
N-Boc-D-pipecolic acid
(R)-N-Boc-哌啶-2-羧酸
(R)-1-N-Boc-哌啶-2-甲酸
(R)-(+)-N-Boc-2-piperidinecarboxylic acid
(S)-N-Boc-piperidine-2-carboxylic Acid
(S)-N-t-Butyloxycarbonyl-piperidine-2-carboxylic Acid
(S)-N-Boc Pipecolic Acid
(2S)-1-[(tert-butyl)oxycarbonyl]piperidine-2-carboxylic Acid
1-t-Butyloxycarbonyl-L-pipecolinic Acid
Boc-D-Pip-OH
N-Boc-D-哌啶-2-羧酸
(R)-1-Boc-piperidine-2-carboxylic acid
(R)-1-Boc-Piperidine-2-carboxylic acid
N-Boc-D-pipecolinic acid
(2R)-1-[(tert-butoxy)carbonyl]piperidine-2-carboxylic acid
Registration numbers
MDL Number
MFCD00237380
MFCD00151904
Beilstein Number
480023
CAS Number
28697-17-8
26250-84-0
PubChem CID
688618
PubChem SID
161002780
24873882
Properties
Product Information
Purity
95+%
Source
98%
Source
95%
Source
Optical Purity
ee: 98% (GLC)
Source
Empirical Formula (Hill Notation)
C11H19NO4
Source
Certificate of Analysis
Download link
Source
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
GHS Signal Word
Warning
Source
German water hazard class
3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Safety Statements
26
-
36
Source
26
-
37
Source
Risk Statements
36/37/38
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
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
Storage Condition
Refrigerator
Source
Physical Property
Melting Point
116-119 °C(lit.)
Source
123-125°C
Source
116-119°C
Source
Optical Rotation
[α]23/D 63.5±3°, c = 1 in acetic acid
Source
+68 , (c=1 in acetic acid)
Source
Apperance
White Solid
Source
Solubility
Methanol
Source
Chloroform
Source
Hydrophobicity(logP)
2.468
Source
Molecule Details
Sigma Aldrich
516341
Packaging
5 g in glass bottle
TRC
B661950
An N-substituted derivative of Pipecolinic Acid useful in modulating ion channel activity.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
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MDL Number
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Beilstein Number
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CAS Number
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PubChem CID
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PubChem SID