58032-84-1

Basic information

• Product Name: 3-NITROPHENYLMETHANESULFONYL CHLORIDE
• Synonyms: 3-nitro-à-toluenesulfonyl chloride;3-Nitro-ɑ-toluenesulfonyl chloride, 95%;3-Nitro-^a-toluenesulfonyl chloride, 95%;3-NitroBenzenemethanesulfonyl chloride;3-Nitrobenzylsulfonyl Chloride;3-nitro-à-toluenesulfonyl chlorid;3-nitro-ɑ-toluenesulfonyl chlorid;3-Nitro-α-toluenesulfonyl chloride
• CAS NO: 58032-84-1
• Molecular Formula: C₇H₆ClNO₄S
• Molecular Weight: 235.64
• Mol File: 58032-84-1.mol
• Article Data: 4

Chemical Properties

• Melting Point: 95-100°C
• Boiling Point: 393.2°C at 760 mmHg
• Flash Point: 191.6°C
• Appearance: /
• Density: 1.57g/cm³
• Vapor Pressure: 4.93E-06mmHg at 25°C
• Refractive Index: 1.596
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• Water Solubility: Reacts with water.
• Sensitive: Moisture Sensitive
• CAS DataBase Reference: 3-NITROPHENYLMETHANESULFONYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-NITROPHENYLMETHANESULFONYL CHLORIDE(58032-84-1)
• EPA Substance Registry System: 3-NITROPHENYLMETHANESULFONYL CHLORIDE(58032-84-1)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21-34-65-22
• Safety Statements: 26-27-36/37/39
• RIDADR: 3261
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 58032-84-1(Hazardous Substances Data)

Usage

Description

3-NITROPHENYLMETHANESULFONYL CHLORIDE, also known as 3-Nitrobenzenemethanesulfonyl chloride, is an organic compound that serves as a versatile reactant or reagent in various organic reactions and synthesis processes. It is characterized by its chemical structure, which includes a nitro group, a phenyl ring, a methanesulfonyl group, and a chloride ion. This unique structure allows it to participate in a wide range of chemical reactions, making it a valuable compound in the field of organic chemistry.

Uses

Used in Organic Chemistry:
3-NITROPHENYLMETHANESULFONYL CHLORIDE is used as a reactant or reagent for facilitating various organic reactions and syntheses. Its application in this field is due to its ability to participate in a wide range of chemical reactions, such as substitution, addition, and elimination reactions, which are essential for the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
3-NITROPHENYLMETHANESULFONYL CHLORIDE is used as an intermediate in the synthesis of pharmaceutical compounds. Its application in this industry is attributed to its reactivity and versatility in organic reactions, which allows for the creation of a diverse range of pharmaceutical compounds with potential therapeutic applications.
Used in Chemical Research:
3-NITROPHENYLMETHANESULFONYL CHLORIDE is used as a research tool in chemical laboratories for studying various organic reactions and mechanisms. Its application in this field is due to its unique chemical structure, which provides researchers with valuable insights into the behavior of different functional groups and their interactions with other molecules.
Used in Material Science:
3-NITROPHENYLMETHANESULFONYL CHLORIDE is used as a building block in the synthesis of novel materials with specific properties. Its application in this industry is based on its ability to form covalent bonds with other molecules, leading to the creation of new materials with unique characteristics, such as improved stability, reactivity, or selectivity.

InChI:InChI=1/C7H6ClNO4S/c8-14(12,13)5-6-2-1-3-7(4-6)9(10)11/h1-4H,5H2

Upstream product

• 553666-72-1 (3-nitrophenyl)methanesulfonic acid 
• 77472-39-0 (3-nitrophenyl)methanethiol 
• 1335107-28-2 ethoxy(((3-nitrophenyl)methyl)sulfanyl)methanethione 
• 1939-99-7 benzenesulfonyl chloride 
• 138564-23-5 Na-salt of 3-nitrobenzylsulfonic acid 
• 619-23-8 3-Nitrobenzyl chloride 

Downstream Products

• 1335107-30-6 (2,2,5-trimethyl-1,3-dioxan-5-yl)methyl (3-nitrophenyl)methanesulfonate 
• 1335107-31-7 (2,2,5-trimethyl-1,3-dioxan-5-yl)methyl (3-aminophenyl)methanesulfonate 
• 1335107-32-8 (2,2,5-trimethyl-1,3-dioxan-5-yl)methyl (3-hydrazinylphenyl)methanesulfonate 
• 1335107-33-9 C₅₁H₆₈N₄O₉S₄ 
• 1073484-58-8 C-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-phenyl}-N-(3-methoxy-propyl)-methanesulfonamide 
• 1073485-39-8 C-(3-amino-phenyl)-N-(3-methoxy-propyl)-methanesulfonamide 
• 1073589-50-0 {3-[4-(2-methoxy-phenyl)-pyrimidin-2-ylamino]-phenyl}-methanesulfonamide 
• 1159281-96-5 C-(3-aminophenyl)-N-[2-(tert-butyldiphenylsilanyloxy)-ethyl]methanesulfonamide 
• 1159281-94-3 N-(2-hydroxyethyl)-C-[3-(2,4,6-trichlorophenylamino)phenyl]methane sulphonamide 
• 1073485-64-9 C-(3-amino-phenyl)-N-(2-hydroxy-ethyl)-methanesulfonamide 
• 1214924-45-4 (1S,2S,3R,4S,5R)-3-(2-chloro-5-fluoropyrimidin-4-ylamino)-5-((3-nitrophenyl)methylsulfonamido)bicyclo[2.2.1]heptane-2-carboxamide 
• 1214924-04-5 (1R,2S,3R,4R,5R)-3-[(2-chloro-5-fluoropyrimidin-4-yl)amino]-5-({[(3-nitrobenzyl)-sulfonyl]amino}methyl)bicyclo[2.2.1]heptane-2-carboxamide 
• 1335490-31-7 C₁₆H₂₇N₃O₄S 
• 1335490-27-1 tert-butyl [4-(((3-((4-chloro-1,3,5-triazin-2-yl)amino)phenyl)methyl)sulfonamido)butyl]carbamate 

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