17700-54-8 Usage
Description
2,6-DICHLOROACETANILIDE is an organic compound with the molecular formula C8H7Cl2N. It is a derivative of acetanilide, featuring two chlorine atoms at the 2' and 6' positions. 2,6-DICHLOROACETANILIDE is known for its potential applications in various fields, particularly in pharmacology and biological studies.
Uses
Used in Pharmacological Activity:
2,6-DICHLOROACETANILIDE is used as a compound for pharmacological activity, specifically in the dynamic method of determination of octanol-water partition coefficient of 2,4-dihydroxythiobenzanilides. This application is crucial for understanding the compound's interaction with biological systems and its potential as a therapeutic agent.
Used in Biological Studies:
In biological studies, 2,6-DICHLOROACETANILIDE serves as a valuable tool for investigating the properties and behavior of various biological systems. Its use in QSAR (Quantitative Structure-Activity Relationship) studies helps researchers predict the biological activity of related compounds, which can be instrumental in drug discovery and development.
Used in QSAR Studies:
2,6-DICHLOROACETANILIDE is used as a reference compound in QSAR studies, which aim to establish a quantitative relationship between the chemical structure of a compound and its biological activity. This information is vital for designing new drugs with improved efficacy and reduced side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 17700-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,0 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17700-54:
(7*1)+(6*7)+(5*7)+(4*0)+(3*0)+(2*5)+(1*4)=98
98 % 10 = 8
So 17700-54-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H7Cl2NO/c1-5(12)11-8-6(9)3-2-4-7(8)10/h2-4H,1H3,(H,11,12)
17700-54-8Relevant articles and documents
Facile synthesis of 2′-acetamido-m-terphenyls via Suzuki coupling
Rajakumar, Perumal,Srisailas, Muthialu
, p. 1811 - 1818 (2004)
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
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Page/Page column 19-20, (2020/10/20)
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
Hajjami, Maryam,Ghorbani-Choghamarani, Arash,Khani, Zahra
, p. 324 - 329 (2013/07/26)
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.