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Molecule
ID:67975
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₁₃NO₂
Molecular Mass
143.18362
Exact Mass
143.09462866
Charge
0
InChI
InChI=1S/C7H13NO2/c1-3-8-4-2-7(1)9-5-6-10-7/h8H,1-6H2
InChIKey
KPKNTUUIEVXMOH-UHFFFAOYSA-N
Canonic Smiles
N1CCC2(CC1)OCCO2
Isomeric Smiles
O1CCOC21CCNCC2
Calculated Properties
JChem
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-2.7245088
LogD (pH = 7.4)
-1.7732062
Log P
0.47091192
Molar Refractivity
36.5912
Polarizability
15.092001
Polar Surface Area
30.49
Rotatable Bonds
0
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
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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
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IUPAC name
Registration numbers
Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR6940
MP Biomedicals
02157858
Sigma Aldrich
178365
Matrix Scientific
073416
Enamine
EN300-30813
Bide Pharmatech
BD10084
Alfa Aesar
A12419
Academic Data
PubChem
67435
Names and Identifiers
Synonyms
1,4-Dioxa-8-azaspiro[4.5]decane
4-Piperidone ethylene ketal 98%
4-Piperidone ethylene ketal
1,4-DIOXA-8-AZASPIRO-(4.5)DECANE
1,4-二叠氮-8-壬烯
1,4-Dioxa-8-azaspiro[4.5]decane
4-Piperidone ethylene acetal
4-哌啶酮缩乙二醇
4-哌啶酮缩乙二醇
4-Piperidone ethylene ketal
1,4-Dioxa-8-azaspiro[4.5]decane
IUPAC Traditional name
1,4-dioxa-8-azaspiro[4.5]decane
IUPAC name
1,4-dioxa-8-azaspiro[4.5]decane
Registration numbers
CAS Number
177-11-7
MDL Number
MFCD00005976
EC Number
205-868-6
PubChem CID
67435
Beilstein Number
506799
PubChem SID
162033707
24850735
Molecule Details
MP Biomedicals
02157858
(4-Piperidone ethylene ketal)
Sigma Aldrich
178365
Packaging
10, 50 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
EC Number
•
PubChem CID
•
Beilstein Number
•
PubChem SID
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
Air Sensitive
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Storage Condition
2-8°C
Source
Safety Statements
S:
20
-
25
-
26
-
37/39
Source
26
-
36
Source
26
-
37
Source
Risk Statements
R:
36/37/38
Source
36/37/38
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
H315
-
H319
-
H335
-
H227
Source
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
GHS Signal Word
Warning
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
P210
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
German water hazard class
3
Source
Product Information
Purity
95+%
Source
98%
Source
95%
Source
98+%
Source
Certificate of Analysis
Download link
Source
Empirical Formula (Hill Notation)
C7H13NO2
Source
Physical Property
Boiling Point
99-100°C/14mm
Source
108-111 °C/26 mmHg(lit.)
Source
99-101°C/14mm
Source
Density
1.17
Source
1.117 g/mL at 20 °C(lit.)
Source
1.117
Source
Flash Point
81°C
Source
81 °C
Source
177.8 °F
Source
81°C(177°F)
Source
n20/D 1.4819(lit.)
Source
1.4819
Source
-0.526
Source
155 - 157°C
Source
Refractive Index
Hydrophobicity(logP)
Melting Point