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Molecule
ID:11760
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₃NO₃
Molecular Mass
171.19372
Exact Mass
171.08954328
Charge
0
InChI
InChI=1S/C8H13NO3/c1-6(10)9-4-2-7(3-5-9)8(11)12/h7H,2-5H2,1H3,(H,11,12)
InChIKey
WFCLWJHOKCQYOQ-UHFFFAOYSA-N
Canonic Smiles
OC(=O)C1CCN(CC1)C(=O)C
Isomeric Smiles
CC(=O)N1CCC(CC1)C(=O)O
Calculated Properties
JChem
Acid pKa
4.426341
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-1.6171569
LogD (pH = 7.4)
-3.3773835
Log P
-0.5098255
Molar Refractivity
42.6412
Polarizability
16.539392
Polar Surface Area
57.61
Rotatable Bonds
1
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
Calculated Properties
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RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
•
IUPAC name
Registration numbers
Properties
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Physical Property
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Product Information
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
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TRC
References
•
PubChem Literature
•
From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR5959
MP Biomedicals
05221567
Matrix Scientific
008731
Life Chemicals
F2190-0008
Sigma Aldrich
647756
TRC
A179540
Bide Pharmatech
BD5417
Alfa Aesar
A15606
Academic Data
PubChem
117255
Names and Identifiers
Synonyms
1-Acetylpiperidine-4-carboxylic acid
Acetylisonipecotic acid
4-Acetylpiperidine-1-carboxylic Acid
N-Acetylpiperidine-4-carboxylic Acid
N-Acetylisonipecotic acid
1-Acetyl-4-piperidinecarboxylic Acid
N-Acetylisonipecotinic acid
1-Acetylisonipecotic Acid
1-ACETYL-4-PIPERIDINECARBOXYLIC ACID
N-乙酰基-4-哌啶羧酸
1-Acetylpiperidine-4-carboxylic acid
1-乙酰基-4-哌啶甲酸
1-乙酰基哌啶-4-羧酸
Ac-DL-Inp-OH
IUPAC Traditional name
1-acetylpiperidine-4-carboxylic acid
IUPAC name
1-acetylpiperidine-4-carboxylic acid
Registration numbers
CAS Number
25503-90-6
MDL Number
MFCD00023706
EC Number
247-049-6
PubChem SID
24883546
160975067
PubChem CID
117255
Beilstein Number
389577
Molecule Details
MP Biomedicals
05221567
MP Biomedicals Rare Chemical collection
Sigma Aldrich
647756
Packaging
5, 25 g in glass bottle
Application
Reactant for synthesis of:
• Triazole derivatives1
• Antiproliferative agents2
• CDK inhibitors3
• CCR5 antagonists for HIV treatment4
• nhNK1 antagonists5
• Piperidine derivatives6
TRC
A179540
Metabolite fingerprinting in transgenic Nicotiana tabacum altered by the Escherichia coli glutamate dehydrogenase gene. A synthetic intermediate in the preparation of CNS depressants.
References
PubChem Literature
From Data Sources
•
Young, J., et al.: Bioorg. Med. Chem. Lett., 17, 5310 (2005)
•
Mungur, R., et al.: J. Biomed. Biotechnol., 2, 198 (2005)
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
EC Number
•
PubChem SID
•
PubChem CID
•
Beilstein Number
Properties
Physical Property
Melting Point
180-183°C
Source
180°C
Source
180-184 °C(lit.)
Source
180-182°C
Source
180-184°C
Source
Partition Coefficient
-0.278
Source
Solubility
Chloroform
来源
Water
Source
Methanol
Source
Apperance
White Solid
Source
Product Information
Purity
98%
Source
95+%
Source
97%
Source
98+%
Source
Certificate of Analysis
Download link
Source
Download link
Source
C8H13NO3
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant
Source
false
Source
否
Source
Warning
Source
Harmful (Xn)
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Source
H302
-
H315
-
H317
-
H319
-
H335
Source
H315
-
H319
-
H335
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
P261
-
P280
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
22
-
36/37/38
-
43
Source
36/37/38
Source
26
-
36
Source
26
-
37
Source
2
Source
Refrigerator
Source
来源
Irritant (Xi)
Source
Source
Empirical Formula (Hill Notation)
TSCA Listed
GHS Signal Word
European Hazard Symbols
Personal Protective Equipment
GHS Hazard statements
GHS Pictograms
GHS Precautionary statements
Risk Statements
Safety Statements
German water hazard class
Storage Condition