Molfinder
主页
技术支持
关于我们
数据来源
数据统计
博客
Molecule
ID:30571
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₁₅N
Molecular Mass
113.2007
Exact Mass
113.12044949
Charge
0
InChI
InChI=1S/C7H15N/c1-6-4-3-5-8-7(6)2/h6-8H,3-5H2,1-2H3
InChIKey
DRLFSUDDXLQHJT-UHFFFAOYSA-N
Canonic Smiles
CC1NCCCC1C
Isomeric Smiles
N1C(C(C)CCC1)C
Calculated Properties
JChem
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
-1.7969215
LogD (pH = 7.4)
-1.4774121
Log P
1.4390355
Molar Refractivity
35.7258
Polarizability
14.445701
Polar Surface Area
12.03
Rotatable Bonds
0
Lipinski's Rule of Five
true
Data Source
Loading...
Names and Identifiers
Loading...
Registration numbers
Loading...
Properties
Loading...
Related Proteins
No Data Available
Click here to submit data
Molecular Spectra
No Data Available
Click here to submit data
Molecule Details
暂无数据
点击上传数据
References
Loading...
Bioactivity
Loading...
Quote
Download
Navigation
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
•
PubChem SID
•
PubChem CID
•
CAS Number
Properties
•
Safety Information
•
Physical Property
•
Product Information
Related Proteins
Molecular Spectra
Molecule Details
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
033227
Enamine
EN300-61154
Academic Data
PubChem
95359
Names and Identifiers
IUPAC name
2,3-dimethylpiperidine
IUPAC Traditional name
2,3-dimethylpiperidine
Synonyms
2,3-Dimethyl-piperidine
2,3-dimethylpiperidine
Registration numbers
MDL Number
MFCD03425894
PubChem SID
160993878
PubChem CID
95359
CAS Number
5347-68-2
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
Physical Property
Hydrophobicity(logP)
1.973
Source
Product Information
95%
Source
Purity