50899-03-1

Basic information

• Product Name: 4-Ethylsulfonylbenzaldehyde
• Synonyms: 4-Ethylsulfonylbenzaldehyde
• CAS NO: 50899-03-1
• Molecular Formula: C₉H₁₀O₃S
• Molecular Weight: 198.2389
• Mol File: 50899-03-1.mol
• Article Data: 10

Chemical Properties

• Melting Point: 108～110℃
• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-Ethylsulfonylbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Ethylsulfonylbenzaldehyde(50899-03-1)
• EPA Substance Registry System: 4-Ethylsulfonylbenzaldehyde(50899-03-1)

Safety Data

• Hazardous Substances Data: 50899-03-1(Hazardous Substances Data)

Usage

General Description

4-Ethylsulfonylbenzaldehyde is a chemical compound with the molecular formula C9H10O2S. It is a pale yellow liquid with a sulfonic acid group and an aldehyde functional group attached to a benzene ring. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. The ethylsulfonyl group provides stability and reactivity to the molecule, making it a useful building block in organic chemistry. It is also employed in the production of dyes, fragrances, and other fine chemicals due to its aromatic properties. Additionally, 4-Ethylsulfonylbenzaldehyde is used in research and development as a versatile reagent for chemical reactions.

Upstream product

• 84211-94-9 4-(ethylthio)benzaldehyde 
• 108129-95-9 4-ethanesulfonyl-benzoyl chloride 
• 100613-79-4 1-ethanesulfonyl-4-diacetoxymethyl-benzene 
• 90561-19-6 1-(bromomethyl)-4-(ethylsulfonyl)benzene 
• 7569-34-8 ethyl p-tolyl sulfone 
• 459-57-4 4-fluorobenzaldehyde 
• 20035-08-9 sodium ethanesulfinate 
• 15164-44-0 p-(iodophenyl)carboxaldehyde 

Downstream Products

• 101655-00-9 1-(4-ethanesulfonyl-benzylidenamino)-imidazolidine-2,4-dione 
• 106883-09-4 isonicotinic acid-(4-ethanesulfonyl-benzylidenehydrazide) 
• 102023-26-7 quinoline-2-carboxylic acid-(4-ethanesulfonyl-benzylidenehydrazide) 
• 100115-29-5 1-(4-ethanesulfonyl-benzylidenamino)-2-thioxo-imidazolidin-4-one 
• 917396-45-3 (4-(ethylsulfonyl)phenyl)methanol 
• 90561-19-6 1-(bromomethyl)-4-(ethylsulfonyl)benzene 
• 84264-83-5 ethyl p-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)propenyl]phenylsulphone 
• 84264-87-9 ethyl p-[2-(1,1,3,3-tetramethyl-5-indanyl)propenyl]phenylsulphone 
• 265114-43-0 5-(4-ethylsulfonylphenyl)-1-(4-methylsulfonylphenyl)imidazole 
• 1026434-15-0 [1-(4-Ethanesulfonyl-phenyl)-meth-(E)-ylidene]-(4-methanesulfonyl-phenyl)-amine 
• 87719-32-2 Etarotene 

Relevant articles and documents

Sulfonylation of Aryl Halides by Visible Light/Copper Catalysis

An efficient visible-light-assisted, copper-catalyzed sulfonylation of aryl halides with sulfinates is reported. In our protocol, a single ligand CuI photocatalyst formed in situ was used in the photocatalytic transformation. Diverse organosulfones were obtained in moderate to good yields. This strategy demonstrates a promising approach toward the synthesis of diverse and useful organosulfones.

1,2,3-BENZOTRIAZOLE DERIVATIVES AS ROR GAMMA T MODULATORS

The present disclosure is directed to compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein ring A, G, L, R1, Rx, Ry, X1, X2, X3, X4, n, p, q and t are

BENZIMIDAZOLE DERIVATIVES AS MODULATORS OF ROR-GAMMA

Provided are novel compounds of Formula I: pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORy. Also provided are pharmaceutical compositions comprising the novel compounds of Formula I and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.