13113-79-6

Basic information

• Product Name: Benzenethiol, 4-nitro-,sodium salt (1:1)
• Synonyms: Benzenethiol,4-nitro-, sodium salt (9CI); Benzenethiol, p-nitro-, sodium deriv. (6CI);Benzenethiol, p-nitro-, sodium salt (8CI); Sodium, [(p-nitrophenyl)thio]-(7CI); 4-Nitrobenzenethiol sodium salt; 4-Nitrothiophenol sodium salt; Sodium4-nitrobenzenethiolate; Sodium 4-nitrophenyl sulfide; Sodium4-nitrothiophenolate; Sodium 4-nitrothiophenoxide; Sodium p-nitrobenzenethiolate;Sodium p-nitrophenylmercaptide; Sodium p-nitrothiophenolate; Sodiump-nitrothiophenoxide; p-Nitrothiophenol sodium salt
• CAS NO: 13113-79-6
• Molecular Formula: C6H5 N O2 S . Na
• Molecular Weight: 177.159
• Mol File: 13113-79-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenethiol, 4-nitro-,sodium salt (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenethiol, 4-nitro-,sodium salt (1:1)(13113-79-6)
• EPA Substance Registry System: Benzenethiol, 4-nitro-,sodium salt (1:1)(13113-79-6)

Safety Data

• Hazardous Substances Data: 13113-79-6(Hazardous Substances Data)

Upstream product

• 15119-62-7 1-acetylsulfanyl-4-nitro-benzene 
• 18803-44-6 sodium p-chlorothiophenolate 
• 1193-00-6 sodium 4-chlorophenolate 
• 1849-36-1 para-nitrobenzenethiol 
• 99234-81-8 S-(4-nitrophenyl) diphenylphosphinothioate 
• 100-00-5 4-chlorobenzonitrile 
• 1223-31-0 bis(4-nitrophenyl)sulfide 

Downstream Products

• 1223-31-0 bis(4-nitrophenyl)sulfide 
• 101291-19-4 2-[(4-nitro-phenylsulfanyl)-methyl]-quinoline 
• 79929-25-2 5-nitro-2-thienyl-4'-nitrophenylsulfide 
• 157563-21-8 4-(4-nitro-phenylsulfanyl)-quinoline-1-oxide 
• 68719-57-3 5-methyl-4-((4-nitrophenyl)thio)-2-phenyl-2,4-dihydro-3H-pyrazol-3-one 
• 92323-58-5 1-nitro-4-(octylsulfanyl)benzene 
• 102160-21-4 1-(4-nitro-phenylsulfanyl)-4-phenyl-phthalazine 
• 5147-64-8 p-nitrobenzenesulfenamide 
• 856980-83-1 1,3-bis-(4-nitro-phenylsulfanyl)-acetone 
• 21387-93-9 4-nitrophenyl 2-nitrophenyl sulfide 
• 100537-48-2 2-((4-nitrophenylthio)methyl)benzothiazole 
• 69127-71-5 4-Nitrophenyl-perfluor-n-propylsulfid 
• 13350-22-6 nitro[4-(prop-2-ynylsulfanyl)]benzene 
• 76928-22-8 C₁₈H₁₈N₂O₆S₃ 

Relevant articles and documents

Solvent effects on reactions of hydroxide ion with phosphorus (V) esters. A quantitative treatment

Second-order rate constants of reactions of HO- with phosphate, phosphinate and thiophosphinate esters, (PhO)2PO.OC6H4NO2-p, Ph2PO.OC6H4NO2-p, Ph2PO.SPh, Ph2PO.SC6H4NO2-p and Ph2PO.SEt, go through minima with decreasing water content of H2O-MeCN or H2O-t-BuOH. The rate decrease is due to stabilization of the non-ionic ester on addition of organic solvent to H2O. This inhibition is partially offset by stabilization of the anionic transition states and in the drier solvents partial desolvation of HO- increases rates.

Structurally homologous sialidases exhibit a commonality in reactivity: Glycoside hydrolase-catalyzed hydrolysis of Kdn-thioglycosides

Aspergillus fumigatus is one of the main causative agents of invasive aspergillosis, an often-lethal fungal disease that affects immunocompromised individuals. A. fumigatus produces a sialidase that cleaves the nine-carbon carbohydrate Kdn from glycoconju

IMIDATE COMPOUND AND USE THEREOF FOR PEST CONTROL

There is provided a compound having an excellent controlling effect on arthropod pests represented by the formula (I-1): wherein Z represents an optionally substituted carbocyclic group or an optionally substituted heterocyclic group; G represents a -A1-R1