17700-54-8

Basic information

• Product Name: 2,6-DICHLOROACETANILIDE
• Synonyms: AKOS 93896;2',6'-DICHLOROACETANILIDE;2,6-DICHLOROACETANILIDE;TIMTEC-BB SBB006286;N-(2,6-DICHLOROPHENYL)ACETAMIDE;2’,6’-dichloro-acetanilid;Acetamide,N-(2,6-dichlorophenyl)-;Acetanilide, 2',6'-dichloro-
• CAS NO: 17700-54-8
• Molecular Formula: C₈H₇Cl₂NO
• Molecular Weight: 204.05
• EINECS: 241-706-0
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 17700-54-8.mol
• Article Data: 12

Chemical Properties

• Melting Point: 180-181°C
• Boiling Point: 343.4°C at 760 mmHg
• Flash Point: 161.5°C
• Appearance: /
• Density: 1.393g/cm³
• Vapor Pressure: 7.08E-05mmHg at 25°C
• Refractive Index: 1.603
• Storage Temp.: Room Temperature
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• PKA: 13.26±0.70(Predicted)
• BRN: 2096165
• CAS DataBase Reference: 2,6-DICHLOROACETANILIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DICHLOROACETANILIDE(17700-54-8)
• EPA Substance Registry System: 2,6-DICHLOROACETANILIDE(17700-54-8)

Safety Data

• Statements: R22:Harmful if swallowed.
• Safety Statements: 22-24/25
• RTECS: AE1970000
• Hazardous Substances Data: 17700-54-8(Hazardous Substances Data)

Usage

Uses

2'',6''-Dichloroacetanilide can be used for pharmacological activity and biological study for dynamic method of determination of octanol-water partition coefficient of 2,4-dihydroxythiobenzanilides in QSAR studies.

InChI:InChI=1/C8H7Cl2NO/c1-5(12)11-8-6(9)3-2-4-7(8)10/h2-4H,1H3,(H,11,12)

Upstream product

• 75-36-5 acetyl chloride 
• 608-31-1 2,6-Dichloroaniline 
• 108-24-7 acetic anhydride 
• 82344-32-9 N-(o-chlorophenyl)-acetohydroxamic acid 
• 10468-16-3 2-chloro-N-hydroxybenzenamine 
• 601-88-7 2,6-dichloronitrobenzene 
• 64-19-7 acetic acid 
• 103-88-8 4-bromoacetanilide 

Downstream Products

• 15178-58-2 p-amino-3,5-dichlorobenzenethiol 
• 23153-07-3 2,6-dichloro-4-(methylthio)aniline 
• 108130-06-9 acetic acid-(2,6-dichloro-4-methylsulfanyl-anilide) 
• 109047-10-1 chloro-acetic acid-(2,6-dichloro-4-methylsulfanyl-anilide) 
• 131732-11-1 N,N-diethyl-glycine-(2,6-dichloro-4-methylsulfanyl-anilide) 
• 13785-48-3 2,6-dichloro-3-nitroaniline 
• 10311-35-0 N-(2,6-dichloro-3-nitrophenyl)acetamide 
• 153466-63-8 2-chloro-N-(2,6-dichlorophenyl)-N-<2H5-phenyl>-acetamide 
• 153466-65-0 o-<(2,6-dichlorophenyl)amino>-<2H4-phenyl>-acetic acid 
• 153466-64-9 1-(2,6-dichlorophenyl)-2-<2H4>-indoline 
• 153466-62-7 N-(2,6-dichlorophenyl)-<2H5>-phenylamine 
• 13953-09-8 4-bromo-2,6-dichloroacetanilide 
• 13277-07-1 3.5-Dichlorsulfanilyl-hydrazid 
• 137090-08-5 N-(2,6-Dichloro-phenyl)-N-methyl-acetamide 

Relevant articles and documents

Facile synthesis of 2′-acetamido-m-terphenyls via Suzuki coupling

Reaction of 2′-amido-m-terphenyl with NaOH and Br2 gave substituted phenanthridinone instead of undergoing rearrangement to give acetamido-m-terphenyl. Thermolysis of 2′-azido-m-terphenyl also gave the phenanthridinone in good yield. The synthesis of 2′-m-terphenyls was accomplished via Suzuki coupling.

SULFONAMIDES AND THEIR USE AS HERBICIDES

The present invention relates to compounds of Formula (I), wherein R1 and R2 are as defined herein. The invention further relates to herbicidal compositions which comprise a compound of Formula (I) and to the use of compounds of Formula (I) for controlling weeds, in particular in crops of useful plants.

L-pyrrolidine-2-carboxylic acid-4-hydrogen sulfate (supported on silica gel) as a new and efficient catalyst for acylation of alcohols, phenols and amines under solvent-free conditions

In the present work, L-pyrrolidine-2-carboxylic acid-4-hydrogen sulfate, supported on silica gel was prepared and characterized by Mass spectroscopy, 1H NMR, 13CNMR, FT IR and elemental analysis (CHN) methods. This heterogenized catalyst can be used as an efficient catalyst for the acylation of alcohols, phenols, and amines with acetic anhydride under mild and solvent-free conditions. Simple work-up, stability of the catalyst, nontoxicity and good to high yields are the advantages of this work.