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Home Halogens 3',4',5-Trichlorosalicylanilide

3',4',5-Trichlorosalicylanilide

CAS No.:
642-84-2
Catalog Number:
AG003IEF
Molecular Formula:
C13H8Cl3NO2
Molecular Weight:
316.5671
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
10g
>98.0%(T)
1 week
United States
$556
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Product Description
Catalog Number:
AG003IEF
Chemical Name:
3',4',5-Trichlorosalicylanilide
CAS Number:
642-84-2
Molecular Formula:
C13H8Cl3NO2
Molecular Weight:
316.5671
MDL Number:
MFCD00059622
IUPAC Name:
5-chloro-N-(3,4-dichlorophenyl)-2-hydroxybenzamide
InChI:
InChI=1S/C13H8Cl3NO2/c14-7-1-4-12(18)9(5-7)13(19)17-8-2-3-10(15)11(16)6-8/h1-6,18H,(H,17,19)
InChI Key:
RSJBLPJKXGNMFW-UHFFFAOYSA-N
SMILES:
Clc1ccc(c(c1)C(=O)Nc1ccc(c(c1)Cl)Cl)O
EC Number:
211-391-4
UNII:
2ZOT9K834Q
NSC Number:
526293
Properties
Complexity:
329  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
314.962g/mol
Formal Charge:
0
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
316.562g/mol
Monoisotopic Mass:
314.962g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
49.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5.2  
Literature
Title Journal
New derivatives of salicylamides: Preparation and antimicrobial activity against various bacterial species. Bioorganic & medicinal chemistry 20131101
Antimycobacterial assessment of Salicylanilide benzoates including multidrug-resistant tuberculosis strains. Molecules (Basel, Switzerland) 20121031
Synthesis and in vitro antimycobacterial activity of 2-methoxybenzanilides and their thioxo analogues. European journal of medicinal chemistry 20121001
Salicylanilide derivatives block Mycobacterium tuberculosis through inhibition of isocitrate lyase and methionine aminopeptidase. Tuberculosis (Edinburgh, Scotland) 20120901
Salicylanilides: selective inhibitors of interleukin-12p40 production. Bioorganic & medicinal chemistry 20080915
Relationship between the structure and antimycobacterial activity of substituted salicylanilides. Archiv der Pharmazie 20030301
Properties