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Molecule
ID:45113
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₆ClNO₃
Molecular Mass
187.58044
Exact Mass
187.00362074
Charge
0
InChI
InChI=1S/C7H6ClNO3/c1-12-5-2-6(8)9-3-4(5)7(10)11/h2-3H,1H3,(H,10,11)
InChIKey
DFXUFJAAXAJWSA-UHFFFAOYSA-N
Canonic Smiles
COc1cc(Cl)ncc1C(=O)O
Isomeric Smiles
c1(c(cc(nc1)Cl)OC)C(=O)O
Calculated Properties
JChem
Acid pKa
4.447529
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
-0.009251126
LogD (pH = 7.4)
-1.772046
Log P
1.0797069
Molar Refractivity
43.4866
Polarizability
16.37306
Polar Surface Area
59.42
Rotatable Bonds
2
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
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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
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RDKit
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IUPAC name
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IUPAC Traditional name
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PubChem CID
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TRC
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Key Organics
KD-0738
TRC
C368730
Bide Pharmatech
BD108842
Matrix Scientific
048589
A&J Pharmtech
AJA-O21516
Academic Data
PubChem
45480411
Names and Identifiers
IUPAC name
6-chloro-4-methoxypyridine-3-carboxylic acid
Synonyms
6-Chloro-4-methoxynicotinic acid
6-Chloro-4-methoxy-3-pyridinecarboxylic Acid
6-Chloro-4-methoxy Nicotinic Acid
IUPAC Traditional name
6-chloro-4-methoxypyridine-3-carboxylic acid
Registration numbers
MDL Number
MFCD10000638
CAS Number
716362-10-6
PubChem CID
45480411
PubChem SID
162049876
Molecule Details
TRC
C368730
Used for preparation of benzimidazolylazabicyclooctylethylpiperidines as Ccr5 antagonists for the treatment of HIV infection.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Product Information
Purity
95+%
Source
>95%
Source
98%
Source
Certificate of Analysis
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Safety Information
MSDS Link
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Source
IRRITANT
Source
false
Source
Storage Warning
TSCA Listed