24524-95-6

Basic information

• Product Name: 4-Nitrothiobenzoic acid S-ethyl ester
• Synonyms: 4-Nitrothiobenzoic acid S-ethyl ester
• CAS NO: 24524-95-6
• Molecular Formula: C₉H₉NO₃S
• Molecular Weight: 211.24
• Mol File: 24524-95-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Nitrothiobenzoic acid S-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Nitrothiobenzoic acid S-ethyl ester(24524-95-6)
• EPA Substance Registry System: 4-Nitrothiobenzoic acid S-ethyl ester(24524-95-6)

Safety Data

• Hazardous Substances Data: 24524-95-6(Hazardous Substances Data)

Upstream product

• 74-96-4 ethyl bromide 
• 122-04-3 4-nitro-benzoyl chloride 
• 75-08-1 ethanethiol 

Downstream Products

• 1151-94-6 4-methoxy-4'-nitrobenzophenone 
• 4792-90-9 copper(I) ethylmercaptide 
• 214360-73-3 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)aniline 
• 1206641-18-0 N-benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline 
• 214360-60-8 N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide 
• 107829-03-8 4-(2-Acetylamino-4-diethylamino-phenylazo)-3,5-dicyano-thiobenzoic acid S-ethyl ester 
• 107829-08-3 4-Amino-3,5-dibrom-thiobenzoesaeure-S-ethylester 
• 62-23-7 4-nitro-benzoic acid 
• 75-08-1 ethanethiol 
• 102879-36-7 4-Amino-thiobenzoesaeure-S-ethylester 

Relevant articles and documents

Rhodium-Catalyzed Decarbonylative Borylation of Aromatic Thioesters for Facile Diversification of Aromatic Carboxylic Acids

Transformation of aromatic thioesters into arylboronic esters was achieved efficiently using a rhodium catalyst. The broad functional-group tolerance and mild conditions of the method have allowed for the two-step decarboxylative borylation of a wide range of aromatic carboxylic acids, including commercially available drugs.

Synthesis and Spectral Characterization of Blue Dyes of the Benzene Series

53 Donor-acceptor substituted azo dyes of the benzene series were prepared by diazonium-coupling reactions (1a-s) or halogen-cyanide exchange (->2a-x, 3a-j).Described are the preparation of the amines 4a-m and the coupling compounds 5a-t and the procedure of diazotizing and coupling.The colouristic and spectroscopic data show that compounds of the general formula 1 are excellent brilliant blue azo dyes usefull for dyeing polyester material.