64399-24-2

Basic information

• Product Name: 4-(METHYLTHIO)-3-NITROBENZOIC ACID
• Synonyms: 3-Nitro-4-methylthiobenzoicacid;4-(Methylthio)-3-nitrobenzoic acid;4-Methylsulfanyl-3-nitrobenzoic acid
• CAS NO: 64399-24-2
• Molecular Formula: C₈H₇NO₄S
• Molecular Weight: 213.21
• Mol File: 64399-24-2.mol
• Article Data: 4

Chemical Properties

• Melting Point: 240 °C(Solv: ethanol (64-17-5))
• Boiling Point: 378.9 °C at 760 mmHg
• Flash Point: 183 °C
• Appearance: /
• Density: 1.48 g/cm³
• Vapor Pressure: 2.04E-06mmHg at 25°C
• Refractive Index: 1.641
• PKA: 3?+-.0.10(Predicted)
• CAS DataBase Reference: 4-(METHYLTHIO)-3-NITROBENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(METHYLTHIO)-3-NITROBENZOIC ACID(64399-24-2)
• EPA Substance Registry System: 4-(METHYLTHIO)-3-NITROBENZOIC ACID(64399-24-2)

Safety Data

• Hazardous Substances Data: 64399-24-2(Hazardous Substances Data)

Usage

General Description

4-(Methylthio)-3-nitrobenzoic acid is a chemical compound with the molecular formula C8H7NO4S. It is a derivative of benzoic acid with a nitro and methylthio substituent. 4-(METHYLTHIO)-3-NITROBENZOIC ACID is commonly used in organic synthesis and as a precursor for pharmaceuticals and agrochemicals. It is also used as a reagent in the production of dyes and pigments. 4-(Methylthio)-3-nitrobenzoic acid is known for its yellow to orange crystalline appearance and its strong odor. It is important to handle and store this chemical with care, as it can be harmful if ingested or inhaled.

InChI:InChI=1/C8H7NO4S/c1-14-7-3-2-5(8(10)11)4-6(7)9(12)13/h2-4H,1H3,(H,10,11)

Upstream product

• 453-71-4 3-nitro-4-fluorobenzoic acid 
• 51919-71-2 4-methylsulfanyl-3-nitro-benzoic acid methyl ester 
• 5188-07-8 sodium thiomethoxide 

Downstream Products

• 873995-55-2 4-methylsulfanyl-3-nitro-benzoyl chloride 
• 51919-71-2 4-methylsulfanyl-3-nitro-benzoic acid methyl ester 
• 141238-13-3 3-amino-4-methylsulfanyl-benzoic acid methyl ester 
• 81029-08-5 4-methylsulfonyl-3-nitro-benzoic acid 
• 1610862-40-2 (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(4-(methylthio)-3-(N-(2-morpholinoethyl)methyl-sulfonamido)benzoyloxy)ethyl)pyridine 1-oxide 
• 1610862-41-3 (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)-phenyl)-2-(3-(methylsulfonamido)-4-(methylthio)benzoyloxy)-ethyl)pyridine 1-oxide 
• 1610862-42-4 (S)-4-(2-(3-amino-4-(methylthio)benzoyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide 
• 1610862-43-5 (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)-phenyl)-2-(4-(methylthio)-3-nitrobenzoyloxy)ethyl)pyridine 1-oxide 

Relevant articles and documents

CHK-, PDK- AND AKT-INHIBITORY PYRIMIDINES, THEIR PRODUCTION AND USE AS PHARMACEUTICAL AGENTS

This invention relates to pyrimidine derivatives of general formula (I) as inhibitors of kinases, their production as well as their use as medications for treating various diseases.

4-Hetaroylpyrazol derivatives and the use thereof as herbicides

Hetaroyl derivatives of the formula I where: R1and R2are each hydrogen, nitro, halogen, cyano, thiocyanato, hydroxyl, mercapto, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-alkylthio, C1-C6-alkylsulfinyl, C1-C6-alkylsulfonyl or C1-C6-alkoxysulfonyl, where the last 6 radicals may be substituted and/or functionalized; phenyl, phenoxy, phenylthio, phenylsulfinyl or phenylsulfonyl, where the last 5 radicals may be substituted; Z is an unsubstituted or substituted four-membered unsaturated, partially or fully saturated chain consisting of three carbons and one nitrogen; Q is unsubstituted or substituted hydroxypyrazole linked at position 4; and their agriculturally useful salts. A process for preparing the hetaroyl derivatives, compositions comprising them, and the use of these derivatives or these compositions comprising them for controlling undesirable plants.