6069-06-3

Basic information

• Product Name: 2-(2-methylphenoxy)-N-[3-nitro-5-(phenylsulfanyl)phenyl]acetamide
• Synonyms: acetamide, 2-(2-methylphenoxy)-N-[3-nitro-5-(phenylthio)phenyl]-
• CAS NO: 6069-06-3
• Molecular Formula: C₄H₉IO
• Molecular Weight: 394.4436
• Mol File: 6069-06-3.mol

Chemical Properties

• Boiling Point: 619.6°C at 760 mmHg
• Flash Point: 328.5°C
• Density: 1.34g/cm³
• Vapor Pressure: 2.79E-15mmHg at 25°C
• Refractive Index: 1.668
• CAS DataBase Reference: 2-(2-methylphenoxy)-N-[3-nitro-5-(phenylsulfanyl)phenyl]acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-methylphenoxy)-N-[3-nitro-5-(phenylsulfanyl)phenyl]acetamide(6069-06-3)
• EPA Substance Registry System: 2-(2-methylphenoxy)-N-[3-nitro-5-(phenylsulfanyl)phenyl]acetamide(6069-06-3)

Safety Data

• Hazardous Substances Data: 6069-06-3(Hazardous Substances Data)

Usage

Molecular weight

360.37 g/mol The mass of one mole of the chemical.

Chemical class

Acetamide The chemical belongs to a class of organic compounds that share a common amide functional group.

Functional groups

Phenoxy, nitro, phenylsulfanyl, acetamide The chemical is composed of several functional groups that give it its unique properties.

Biological activity

Potential The chemical may have biological activities that make it valuable for further exploration and development.

Research applications

Various The chemical is used in a range of research studies, but its specific applications are not detailed in the material provided.

Pharmaceutical industry

Potential applications The chemical may have potential uses in the pharmaceutical industry, but further research and testing are necessary to fully understand its potential.

Upstream product

• 64-17-5 ethanol 
• 624-73-7 1,2-Diiodoethane 
• 628-34-2 2-chloroethyl ethyl ether 
• 110-80-5 2-ethoxy-ethanol 
• 17178-11-9 2-ethoxyethyl p-toluenesulfonate 

Downstream Products

• 109185-18-4 acetic acid-[4-(2-ethoxy-ethoxy)-anilide] 
• 109-92-2 ethyl vinyl ether 
• 2141-62-0 3-(ethoxy)propionitrile 
• 628-34-2 2-chloroethyl ethyl ether 
• 592-55-2 2-Bromoethyl ethyl ether 
• 26311-17-1 [N₁₁,2O₂] 
• 109185-17-3 acetic acid-[2-(2-ethoxy-ethoxy)-anilide] 
• 105838-39-9 (2-ethoxy-ethyl)-ethyl-phenyl-phosphine 
• 31680-53-2 [4-(2-Ethoxy-ethylamino)-2,3-dimethyl-phenyl]-phenyl-methanone 
• 16332-51-7 (3-oxapentyl)trimethylammonium iodide 
• 1027905-16-3 {[4-(2-Ethoxy-ethoxy)-benzenesulfonyl]-isobutyl-amino}-acetic acid ethyl ester 
• 598-32-3 2-hydroxy-3-butene 
• 1192717-23-9 diethyl 1-(2-ethoxyethyl)-5-methyl-3-phenyl-1H-pyrrole-2,4-dicarboxylate 
• 101787-42-2 (4-ethoxybutane-1,1-diyl)dibenzene 

Relevant articles and documents

PYRROLE ANTIFUNGAL AGENTS

The invention provides compounds of formula (I), and pharmaceutically and agriculturally acceptable salts thereof; wherein: R1, R2, R3, R4, R5, R6, A1, L1 and n are as defined herein. These compounds and their pharmaceutically acceptable salts are useful in prevention or treatment of a fungal disease. Compounds of formula (I), and agriculturally acceptable salts thereof, may also be used as agricultural fungicides.

Triphenylphosphine/2,3-dichloro-5,6-dicyanobenzoquinone as a new, selective and neutral system for the facile conversion of alcohols, thiols and selenols to alkyl halides in the presence of halide ions

A mixture of triphenylphosphine (Ph3P) and 2,3-dichloro-5,6-dicyanobenzoquinone in CH2Cl2 affords a complex which in the presence of R4NX (X=Cl, Br, I) converts alcohols, thiols and selenols into their corresponding alkyl halides in high yields at room temperature. The method is highly selective for the conversion of 1° alcohols in the presence of 2° ones and also 1° and 2° alcohols in the presence of 3° alcohols, thiols, epoxides, trimethylsilyl- and tetrahydropyranyl ethers, 1,3 dithianes, disulfides, and amides.

Synthesis and Photochromism of Crowned Spirobenzothiapyran: Facilitated Photoisomerization by Cooperative Complexation of Crown Ether and Thiophenolate Moieties with Metal Ions

Spirobenzothiapyrans bearing monoaza-12-crown-4, -15-crown-5, -18-crown-6, and oligooxyethylene moieties were synthesized, and their photochromism was examined in the presence of cations in acetonitrile. The cation complexation by their crown ether moieties cannot induce thermal isomerization to their corresponding colored merocyanine form, unlike the corresponding spirobenzopyran derivatives. The UV-light-induced isomerization was, however, facilitated by the cation complexation of the crown ether moieties and the affinity of the merocyanine thiophenolate anion to metal ions, especially in the presence of Li+ and Ag+. The presence of Ag+ brought about the most remarkable effect in the facilitation of photoisomerization of the spirobenzothiapyrans and the thermal stability of the colored merocyanine form mainly due to the powerful interaction of the thiophenolate anion with the soft metal ion.