1159512-27-2

Basic information

• Product Name: 3-Amino-4-hydroxyphenylsulphur pentafluoride
• Synonyms: 3-Amino-4-hydroxypentafluorosulphanylbenzene;3-Amino-4-hydroxyphenylsulphur pentafluoride;2-Amino-4-(pentafluorosulphanyl)phenol, 2-Hydroxy-5-(pentafluorothio)aniline;(3-Amino-4-hydroxyphenyl)sulfur pentafluoride;2-Amino-4-(pentafluorosulfanyl)phenol;2-amino-4-(pentafluoro-$l^{6}-sulfanyl)phenol
• CAS NO: 1159512-27-2
• Molecular Formula: C₆H₆F₅NOS
• Molecular Weight: 235.174956
• Mol File: 1159512-27-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-Amino-4-hydroxyphenylsulphur pentafluoride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Amino-4-hydroxyphenylsulphur pentafluoride(1159512-27-2)
• EPA Substance Registry System: 3-Amino-4-hydroxyphenylsulphur pentafluoride(1159512-27-2)

Safety Data

• Hazard Codes: Xi,T
• Statements: 36/37/38
• Safety Statements: 26
• Hazardous Substances Data: 1159512-27-2(Hazardous Substances Data)

Upstream product

• 1159512-26-1 2-nitro-4-(pentafluorosulfanyl)phenol 
• 2613-26-5 3-nitrophenylsulfur pentafluoride 
• 774-94-7 4-(pentafluoro-λ⁶-sulfaneyl)phenol 

Relevant articles and documents

WDR5-MYC INHIBITORS

Substituted N-phenyl sulfonamide compounds inhibit WDR5-MYC interactions, and the compounds and their pharmaceutical compositions are useful for treating disorders and conditions in a subject, such as cancer cell proliferation.

BICYCLIC HETEROARYL DERIVATIVES AND PREPARATION AND USES THEREOF

Compounds of Formula (A), where the definition of the variables are as described in the description, as well as their preparation and uses, and pharmaceutical compositions comprising these compounds and their uses as modulators of dysfunctional glutamate

Hydroxylation of nitro-(pentafluorosulfanyl)benzenes via vicarious nucleophilic substitution of hydrogen

Para- and meta-nitro-(pentafluorosulfanyl)benzenes react with anions of cumyl hydroperoxide in the presence of t-BuOK in liquid ammonia to form nitro-(pentafluorosulfanyl)phenols. Their reduction with hydrogen in the presence of Raney-Nickel provides amin