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ChemicalBook--->CAS DataBase List--->25984-63-8

25984-63-8

25984-63-8 Structure

25984-63-8 Structure
IdentificationMore
[Name]

4-HYDROXYTHIOBENZAMIDE
[CAS]

25984-63-8
[Synonyms]

4-HYDROXYTHIOBENZAMIDE
4-Hydroxy Thiobenzamide p-Hydroxy Thiobenzamide
p-HydroxyThioBenzamide
4-hydroxybenzothioamide
4-HYDROXY THIOBENZAMIDE 98.0%MIN
[EINECS(EC#)]

674-712-0
[Molecular Formula]

C7H7NOS
[MDL Number]

MFCD04973332
[Molecular Weight]

153.2
[MOL File]

25984-63-8.mol
Questions And AnswerBack Directory
[Uses]

4-Hydroxythiobenzamide(25984-63-8) is used in the synthesis of PPARα agonists used in increasing HDLc levels. Also used in the synthesis of potent CDK5 inhibitors in the treatment of Alzheimer’s disease.
Chemical PropertiesBack Directory
[Melting point ]

181-185℃
[Boiling point ]

320.4±44.0 °C(Predicted)
[density ]

1.338±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

9.24±0.26(Predicted)
[color ]

Light Yellow
[InChI]

InChI=1S/C7H7NOS/c8-7(10)5-1-3-6(9)4-2-5/h1-4,9H,(H2,8,10)
[InChIKey]

VDTNKXSVUGXUOJ-UHFFFAOYSA-N
[SMILES]

C1(C(N)=S)=CC=C(O)C=C1
[CAS DataBase Reference]

25984-63-8(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[HS Code ]

29242990
Hazard InformationBack Directory
[Chemical Properties]

4-Hydroxythiobenzamide has an appearance ranging from light orange to yellow to green, powder to crystalline, melting point 192 °C, soluble in methanol.
[Synthesis]

4-Hydroxythiobenzamide is an important intermediate of Febuxostat, a new anti-gout drug. A patent discloses a method for preparing p-hydroxythiobenzamide. Specifically, a certain amount of water, p-cyanophenol, sodium hydrosulfide, and secondary amine are mixed evenly. At a specific temperature, an organic weak acid is added dropwise. After the reaction is completed, the mixture is filtered, and the filter cake is dried to obtain 4-Hydroxythiobenzamide.
4-HYDROXYTHIOBENZAMIDE
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