Molfinder
Home
Support
About Us
Data Source
Statistics
Blogs
Molecule
ID:118698
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₅H₁₃N₃O₂
Molecular Mass
267.28262
Exact Mass
267.10077667
Charge
0
InChI
InChI=1S/C15H13N3O2/c1-9-8-12(15(19)20)16-14-13(10(2)17-18(9)14)11-6-4-3-5-7-11/h3-8H,1-2H3,(H,19,20)
InChIKey
FAMCLLZNSYFZQT-UHFFFAOYSA-N
Canonic Smiles
Cc1nn2c(c1c1ccccc1)nc(cc2C)C(=O)O
Isomeric Smiles
c12n(nc(c1c1ccccc1)C)c(cc(n2)C(=O)O)C
Calculated Properties
JChem
Acid pKa
3.3501086
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
0.5174731
LogD (pH = 7.4)
-0.745617
Log P
2.476763
Molar Refractivity
85.5352
Polarizability
29.196585
Polar Surface Area
67.49
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
•
MDL Number
•
PubChem CID
•
PubChem SID
Properties
•
Physical Property
•
Product Information
Related Proteins
Molecular Spectra
Molecule Details
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Life Chemicals
F3250-0737
InterBioScreen
BB_SC-3337
Enamine
EN300-111077
Academic Data
PubChem
7061944
Names and Identifiers
IUPAC name
2,7-dimethyl-3-phenylpyrazolo[1,5-a]pyrimidine-5-carboxylic acid
Synonyms
2,7-dimethyl-3-phenylpyrazolo[1,5-a]pyrimidine-5-carboxylic acid
IUPAC Traditional name
2,7-dimethyl-3-phenylpyrazolo[1,5-a]pyrimidine-5-carboxylic acid
Registration numbers
MDL Number
MFCD07636875
PubChem CID
7061944
PubChem SID
162098515
Properties
Physical Property
Partition Coefficient
2.187
Source
Hydrophobicity(logP)
3.065
Source
Product Information
Purity
95+%
Source
95%
Source
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay