Molfinder
主页
技术支持
关于我们
数据来源
数据统计
博客
Molecule
ID:40231
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₆ClNO₂S
Molecular Mass
239.67814
Exact Mass
238.98077712
Charge
0
InChI
InChI=1S/C10H6ClNO2S/c11-7-3-1-6(2-4-7)9-12-8(5-15-9)10(13)14/h1-5H,(H,13,14)
InChIKey
OOINMGFADWPJPC-UHFFFAOYSA-N
Canonic Smiles
Clc1ccc(cc1)c1scc(n1)C(=O)O
Isomeric Smiles
c1(nc(sc1)c1ccc(cc1)Cl)C(=O)O
Calculated Properties
JChem
Acid pKa
3.1771157
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
1.0028733
LogD (pH = 7.4)
-0.14556868
Log P
3.3042867
Molar Refractivity
68.057
Polarizability
22.654806
Polar Surface Area
50.19
Rotatable Bonds
2
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
•
Synonyms
•
IUPAC Traditional name
Registration numbers
•
PubChem CID
•
MDL Number
•
PubChem SID
•
CAS Number
Properties
•
Physical Property
•
Safety Information
•
Product Information
Related Proteins
Molecular Spectra
Molecule Details
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Maybridge
MO01132
Key Organics
12F-339S
Matrix Scientific
043214
Enamine
EN300-15223
A&J Pharmtech
AJA-O39143
Academic Data
PubChem
673682
Names and Identifiers
IUPAC name
2-(4-chlorophenyl)-1,3-thiazole-4-carboxylic acid
Synonyms
2-(4-Chlorophenyl)-1,3-thiazole-4-carboxylic acid
IUPAC Traditional name
2-(4-chlorophenyl)-1,3-thiazole-4-carboxylic acid
Registration numbers
PubChem CID
673682
MDL Number
MFCD00142032
PubChem SID
162044994
CAS Number
17228-98-7
Properties
Physical Property
Melting Point
187-190°C
Source
187 - 190 °C
Source
Hydrophobicity(logP)
3.865
Source
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
Product Information
Purity
>95%
Source
97%
Source
95%
Source
98%
Source
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay