70102-34-0

Basic information

• Product Name: 3-NITRO-THIOBENZAMIDE
• Synonyms: 3-NITRO-THIOBENZAMIDE;3-Nitrobenzothioamide;Benzenecarbothioamide, 3-nitro-;3-nitrobenzenecarbothioamide
• CAS NO: 70102-34-0
• Molecular Formula: C₇H₆N₂O₂S
• Molecular Weight: 182.2
• Mol File: 70102-34-0.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 336.339°C at 760 mmHg
• Flash Point: 157.212°C
• Appearance: /
• Density: 1.425g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.692
• CAS DataBase Reference: 3-NITRO-THIOBENZAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-NITRO-THIOBENZAMIDE(70102-34-0)
• EPA Substance Registry System: 3-NITRO-THIOBENZAMIDE(70102-34-0)

Safety Data

• Hazardous Substances Data: 70102-34-0(Hazardous Substances Data)

Usage

Description

3-NITRO-THIOBENZAMIDE, with the molecular formula C7H6N2O3S, is a yellow solid chemical compound that possesses a molecular weight of 198.20 g/mol. Characterized by its nitro and thio groups, this compound is versatile for use in various chemical processes and is commonly found in organic synthesis, pharmaceutical research and development, as well as in the production of agrochemicals and dyes. However, due to its potential health and environmental hazards, careful handling is required.

Uses

Used in Organic Synthesis:
3-NITRO-THIOBENZAMIDE is used as a reagent in organic synthesis for its ability to participate in a range of chemical reactions, facilitating the creation of diverse chemical products.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, 3-NITRO-THIOBENZAMIDE is utilized as a key intermediate in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Production:
3-NITRO-THIOBENZAMIDE is employed as a component in the production of agrochemicals, playing a role in the development of products designed to enhance crop protection and yield.
Used in Dye Manufacturing:
3-NITRO-THIOBENZAMIDE is also used in the manufacturing of dyes, where its chemical properties contribute to the creation of various colorants for different applications.

InChI:InChI=1/C7H6N2O2S/c8-7(12)5-2-1-3-6(4-5)9(10)11/h1-4H,(H2,8,12)

Upstream product

• 507-09-5 thioacetic acid 
• 619-24-9 3-nitrobenzonitrile 
• 66907-51-5 3-nitrobenzyl thiocyanate 
• 645-09-0 3-nitrobenzamide 
• 619-23-8 3-Nitrobenzyl chloride 
• 99-61-6 3-nitro-benzaldehyde 
• 121-92-6 3-nitrobenzoic acid 
• 879905-34-7 3-nitro-benzaldehyde imine 

Downstream Products

• 29947-37-3 2-[2-(3-nitro-phenyl)-thiazol-4-yl]-benzothiazole 
• 29942-10-7 6-[2-(3-nitro-phenyl)-thiazol-4-yl]-benzothiazole 
• 76659-40-0 2-(3-nitro-phenyl)-thiazolo[4,5-b]quinoxaline 
• 77472-39-0 (3-nitrophenyl)methanethiol 
• 250258-61-8 2-{2-[2-(3-nitro-phenyl)-thiazol-4-yl]-ethyl}-isoindole-1,3-dione 
• 121262-07-5 2-(3-nitrophenyl)thiazole-4-carboxylic acid ethyl ester 
• 460750-31-6 2-(3-aminophenyl)thiazole-4-carboxylic acid amide 
• 92057-32-4 2-(3-nitro-phenyl)-thiazole-4-carboxylic acid 
• 460750-30-5 2-(3-nitrophenyl)thiazole-4-carboxylic acid amide 
• 105361-75-9 2‐(3‐nitrophenyl)‐1,3‐thiazole 
• 15911-29-2 4-methyl-2-(3-nitrophenyl)-5-thiazolecarboxylic acid 
• 1259389-16-6 4-(furan-2-yl)-2-(3-nitrophenyl)thiazole 
• 96159-88-5 2-(3-nitrophenyl)-4,5-dihydro-1,3-thiazole 
• 106537-77-3 3,5-bis(3-nitrophenyl)-1,2,4-thiadiazole 

Relevant articles and documents

Mo (CO)6-assisted Pd-supported magnetic graphene oxide-catalyzed carbonylation-cyclization as an efficient way for the synthesis of 4(3H)-quinazolinones

In this paper, a novel catalyst is introduced based on the immobilization of palladium on modified magnetic graphene oxide nanoparticles. The catalyst is characterized by several methods, including transmission electron microscopy, scanning electron microscopy, X-ray fluorescence, vibrating-sample magnetometer, Fourier transform-infrared and dynamic light scattering (DLS) analysis. The activity of the catalyst was investigated in the synthesis of 4(3H)-quinazolinones via Pd-catalyzed carbonylation-cyclization of N-(2-bromoaryl) benzimidamides by Mo (CO)6. The Mo (CO)6 is used as a carbon monoxide source for performing the reaction under mild conditions. The catalyst showed good reusability, and no change in activity was observed after 10?cycles of recovery.

Crystal landscape of primary aromatic thioamides

The crystal landscape of a series of primary aromatic thioamides is described, displaying similar characteristic intermolecular hydrogen-bonding interactions in the solid state to those observed in their widely studied amide analogues, including R22(8) dimers and C(4) chains. In a number of cases, high Z′ values were observed in the structures. On the basis of the observed solid-state features, the thioamide functional group, which is a strong hydrogen-bond donor and moderate acceptor, offers considerable potential as a key moiety for crystal engineering.

Sulfonic acid functionalized nano Γ-Al 2O 3: A new, efficient, and reusable catalyst for synthesis of thioamides

Sulfonic acid functionalized nano γ-Al2O3 is easily prepared by the reaction of nano γ-Al2O3 with 1,3-propane sulfone. This reagent can be used as an eficient catalyst for the synthesis of thioamides. This new method consistently has the advantages of excellent yields and short reaction times. Further, the catalyst can be recovered for several times.