24167-52-0

Basic information

• Product Name: 3-Chloro-N,N-diMethylbenzaMide, 97%
• Synonyms: 3-Chloro-N,N-diMethylbenzaMide, 97%;BenzaMide, 3-chloro-N,N-diMethyl-
• CAS NO: 24167-52-0
• Molecular Formula: C₉H₁₀ClNO
• Molecular Weight: 183.6348
• Mol File: 24167-52-0.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-Chloro-N,N-diMethylbenzaMide, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Chloro-N,N-diMethylbenzaMide, 97%(24167-52-0)
• EPA Substance Registry System: 3-Chloro-N,N-diMethylbenzaMide, 97%(24167-52-0)

Safety Data

• Hazardous Substances Data: 24167-52-0(Hazardous Substances Data)

Upstream product

• 618-46-2 m-Chlorobenzoyl chloride 
• 124-40-3 dimethyl amine 
• 108-41-8 1-chloro-3-methylbenzene 
• 68-12-2 N,N-dimethyl-formamide 
• 137-26-8 Thiram 
• 535-80-8 3-chlorobenzoate 
• 587-04-2 m-Chlorobenzaldehyde 
• 937-14-4 3-chloro-benzenecarboperoxoic acid 
• 13360-57-1 dimethylamino sulfonyl chloride 
• 78162-58-0 N,N-dimethyl-1H-imidazole-1-sulfonamide 
• 873-63-2 m-chlorobenzyl alcohol 

Downstream Products

• 63833-37-4 5-(3-chloro-benzoyl)-2,4-dimethyl-pyrrole-3-carboxylic acid ethyl ester 
• 1369884-55-8 C₁₁H₆Cl₂N₂O 
• 587-04-2 m-Chlorobenzaldehyde 
• 1613045-48-9 (Z)-N-(1-(3-chlorophenyl)-1-(dimethylamino)-3-oxo-3-phenylprop-1-en-2-yl)-4-methylbenzenesulfonamide 
• 1613045-49-0 C₂₄H₂₃ClN₂O₃S 
• 15184-97-1 1-(3-chlorophenyl)-N,N-dimethylmethanamine 
• 404009-46-7 AMA₃₇ 
• 90-94-8 bis(p-dimethylaminophenyl)methanone 
• 2125473-29-0 2-chloro-4-(3-chlorophenyl)-6-phenyl-1,3,5-triazine 
• 1154642-19-9 1-(3-chlorophenyl)-2-(phenylthio)ethanone 
• 1446279-87-3 (E)-5-chloro-N,N-dimethyl-2-(prop-1-en-1-yl)benzamide 
• 1446279-89-5 (E)-3-chloro-N,N-dimethyl-2-(prop-1-en-1-yl)benzamide 
• 622372-94-5 (2-bromopyridin-3-yl)(3-chlorophenyl)methanone 
• 89604-36-4 1-<3-chloro-2-(methylthio)phenyl>ethanone 

Relevant articles and documents

One-pot synthesis of a highly disperse core-shell CuO-alginate nanocomposite and the investigation of its antibacterial and catalytic properties

In this study, sodium alginate was extracted from Sargassum algae, collected from coastal waters of Bushehr, Persian Gulf, Iran and used as a stabilizing and wrapping agent for CuO nanoparticles. The synthesized nanocomposite was characterized by some spectroscopic and microscopic techniques, such as IR, XRD, Uv-vis, BET, BJH, zeta potential, SEM, TEM, HR-TEM, and XPS. The antibacterial effects of the CuO-alginate nanocomposite against some bacteria, isolated from a burn wound, were evaluated. The results showed that this nanocomposite had better antibacterial effects than its components onPseudomonas aeruginosaATCC 27853,Staphylococcus aureusATCC 12600,Streptococcus pyogenesATCC 19615, andStaphylococcus epidermidisATCC 49461. Among these,Staphylococcus aureusATCC 12600 was the most sensitive one to this nanocomposite, with the lowest minimum inhibitory concentration (2.08 mg mL?1) observed. Moreover, the synthesized nanocomposite showed good catalytic activity in the oxidative coupling of carboxylic acids withN,N-dialkylformamides toward the synthesis of amides.

NOVEL HETEROCYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

Provided is a heterocyclic compound Chemical Formula 1 or 2: and an organic light emitting device comprising the same.

Preparation of Thioanisole Biscarbanion and C-H Lithiation/Annulation Reactions for the Access of Five-Membered Heterocycles

The synthesis, isolation, and X-ray structure of a thioanisole-based trilithium complex are reported. On the basis of the double-lithiation strategy, two novel synthetic methodologies have been developed under mild reaction conditions (room temperature): (1) reactions of lithiated thioanisoles with nitriles give benzoisothiazoles via a [3 + 2]-type of approach with two new bond formations and (2) formation of benzothiophenes from thioanisoles and amides through a [4 + 1] pattern forming 4 new chemical bonds.