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63547-24-0 molecular structure
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2-diphenylmethanesulfinylacetic acid

ChemBase ID: 174675
Molecular Formular: C15H14O3S
Molecular Mass: 274.33486
Monoisotopic Mass: 274.06636531
SMILES and InChIs

SMILES:
c1ccccc1C(S(=O)CC(=O)O)c1ccccc1
Canonical SMILES:
OC(=O)CS(=O)C(c1ccccc1)c1ccccc1
InChI:
InChI=1S/C15H14O3S/c16-14(17)11-19(18)15(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,15H,11H2,(H,16,17)
InChIKey:
QARQPIWTMBRJFX-UHFFFAOYSA-N

Cite this record

CBID:174675 http://www.chembase.cn/molecule-174675.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
2-diphenylmethanesulfinylacetic acid
IUPAC Traditional name
diphenylmethanesulfinylacetic acid
Synonyms
2-[(Diphenylmethyl)sulfinyl]acetic Acid
Modafinil Acid
Modafinic Acid
Modafinil Carboxylate
CAS Number
63547-24-0
PubChem SID
164230585
PubChem CID
3085267

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC M482510 external link Add to cart
PubChem 3085267 external link
Data Source Data ID Price
TRC
M482510 external link Add to cart Please log in.
Data Source Data ID
PubChem 3085267 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 4.0638003  H Acceptors
H Donor LogD (pH = 5.5) 0.89144456 
LogD (pH = 7.4) -0.7815634  Log P 2.339777 
Molar Refractivity 75.5664 cm3 Polarizability 29.565556 Å3
Polar Surface Area 54.37 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
DMSO expand Show data source
Methanol expand Show data source
Apperance
Off-White to Pale Pink Solid expand Show data source
Melting Point
130-132°C expand Show data source
Storage Condition
-20°C Freezer expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
Download expand Show data source

DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - M482510 external link
A metabolite of Modafinil, a central nervous system vigilance promoting agent, which possesses neuroprotective properties.

REFERENCES

REFERENCES

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  • • Duteil, J., et al.: Eur. J. Pharmacol., 180, 49 (1990)
  • • Wong, Y., et al.: J. Clin. Pharmacol., 317, 30 (1990)
  • • Robertson, P., et al.: Drug Disp., 42, 123 (2003)
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PATENTS

PATENTS

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INTERNET

INTERNET

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