102117-40-8

Basic information

• Product Name: 3,5-Bis(trifluoromethylthio)benzoic acid
• Synonyms: 3,5-Bis(trifluoromethylthio)benzoic acid
• CAS NO: 102117-40-8
• Molecular Formula: C₉H₄F₆O₂S₂
• Molecular Weight: 322.2472792
• Mol File: 102117-40-8.mol
• Article Data: 2

Chemical Properties

• Melting Point: 103-105℃
• Boiling Point: 225.5°C at 760 mmHg
• Flash Point: 90.2°C
• Appearance: /
• Density: 1.67g/cm³
• Vapor Pressure: 0.049mmHg at 25°C
• Refractive Index: 1.524
• CAS DataBase Reference: 3,5-Bis(trifluoromethylthio)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Bis(trifluoromethylthio)benzoic acid(102117-40-8)
• EPA Substance Registry System: 3,5-Bis(trifluoromethylthio)benzoic acid(102117-40-8)

Safety Data

• Hazardous Substances Data: 102117-40-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H4F6O2S2/c10-8(11,12)18-5-1-4(7(16)17)2-6(3-5)19-9(13,14)15/h1-3H,(H,16,17)

Upstream product

• 21829-31-2 3,5-bis-chlorosulfonyl-benzoic acid 
• 2314-97-8 iodotrifluoromethane 
• 102117-39-5 3,5-dimercaptobenzoic acid 

Downstream Products

• 102117-41-9 3,5-bis(trifluoromethylsulfonyl)benzoic acid 
• 111222-78-7 3,5-Bis(trifluoromethylsulfonyl)acetanilide 
• 80121-01-3 3,5-bis(trifluoromethylsulfonyl)-1-chlorobenzene 
• 102117-52-2 3,5-bis(trifluoromethylsulfonyl)phenol 
• 111222-77-6 3,5-Bis(trifluoromethylthio)acetanilide 
• 102117-54-4 3,5-bis(trifluoromethylsulfonyl)phenyl p-toluenesulfonate 
• 102117-53-3 3,5-bis(trifluoromethylsulfonyl)phenyl trifluoromethanesulfonate 
• 102117-45-3 3,5-bis(trifluoromethylsulfonyl)benzamide 
• 102117-44-2 3,5-bis(trilfuoromethylsulfonyl)benzonitrile 
• 102117-51-1 3,5-bis(trifluoromethylsulfonyl)iodobenzene 
• 102117-50-0 3,5-bis(trifluoromethylsulfonyl)-1-bromobenzene 
• 102117-49-7 3,5-bis(trifluoromethylsulfonyl)-1-fluorobenzene 
• 102117-42-0 3,5-bis(trifluoromethylthio)benzamide 
• 102117-43-1 3,5-bis(trifluoromethylthio)benzonitrile 

Relevant articles and documents

N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY

Novel N-hydroxyamide derivatives are disclosed. These N-hydroxyamide derivatives inhibit UPD-3O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase, an enzyme present in gram negative bacteria and are therefore useful as antimicrobials and antibiotics. Methods of synthesis and of use of the compounds are also disclosed.