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5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide 2-aminoethanol salt - 98%, high purity , CAS No.1420-04-8

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5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide 2-aminoethanol salt - 98%, high purity , CAS No.1420-04-8

COA

Grade & Purity:

≥98%

Cas Number: 1420-04-8
Molecular Weight: 388.2
EC Number: ‘215-811-7
PubChem CID: 14992

In stock

Item Number

C587196

Grouped product items
SKU	Size	Availability	Price
C587196-25g	25g	2	$10.90
C587196-100g	100g	2	$23.90
C587196-500g	500g	1	$104.90

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Antibiotic (1629) JAK/STAT Signaling (507) Parasite (997) STAT (139) Stem Cell/Wnt (1019)

Basic Description

Synonyms	Phenasal ethanolamine salt \| SCHEMBL1871351 \| Niclosamide-olamine \| Ethanolamine salt of 5,2'-dichloro-4'-nitrosalicyclicanilide \| 2',5-Dichloro-4'-nitrosalicylanilide, 2-aminoethanol salt \| Baylucit \| Clonitralid \| Niclosamide (olamine) \| UNII-QT8YUD1Z0W
Specifications & Purity	≥98%
Storage Temp	Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Anilides
      - Level5 Aromatic anilides
        Level6 Benzanilides

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Anilides
Intermediate Tree Nodes	Aromatic anilides
Direct Parent	Benzanilides
Alternative Parents	3-halobenzoic acids and derivatives Salicylamides Benzamides Nitrobenzenes Benzoyl derivatives Nitroaromatic compounds P-chlorophenols 1-hydroxy-2-unsubstituted benzenoids Chlorobenzenes Aryl chlorides Vinylogous acids 1,2-aminoalcohols Secondary carboxylic acid amides Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Organochlorides Organic zwitterions Organic oxides Monoalkylamines Hydrocarbon derivatives Organopnictogen compounds Primary alcohols
Molecular Framework	Not available
Substituents	Benzanilide - Salicylamide - Salicylic acid or derivatives - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Nitrobenzene - Benzoic acid or derivatives - Benzamide - Benzoyl - Nitroaromatic compound - 4-halophenol - 4-chlorophenol - Chlorobenzene - Halobenzene - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aryl halide - Aryl chloride - Vinylogous acid - Carboxamide group - Secondary carboxylic acid amide - 1,2-aminoalcohol - C-nitro compound - Organic nitro compound - Alkanolamine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Primary aliphatic amine - Primary amine - Organic zwitterion - Amine - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary alcohol - Organooxygen compound - Organohalogen compound - Organic oxygen compound - Organochloride - Organonitrogen compound - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as benzanilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with a benzene ring. They have the general structure RNC(=O)R', where R,R'= benzene.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Schistosoma japonicum (780 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	2-aminoethanol;5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide
INCHI	InChI=1S/C13H8Cl2N2O4.C2H7NO/c14-7-1-4-12(18)9(5-7)13(19)16-11-3-2-8(17(20)21)6-10(11)15;3-1-2-4/h1-6,18H,(H,16,19);4H,1-3H2
InChIKey	XYCDHXSQODHSLG-UHFFFAOYSA-N
Smiles	C1=CC(=C(C=C1[N+](=O)[O-])Cl)NC(=O)C2=C(C=CC(=C2)Cl)O.C(CO)N
Isomeric SMILES	C1=CC(=C(C=C1[N+](=O)[O-])Cl)NC(=O)C2=C(C=CC(=C2)Cl)O.C(CO)N
Molecular Weight	388.2
Reaxy-Rn	4078572
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4078572&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number	Certificate Type	Date	Item
H2323106	Certificate of Analysis	Aug 03, 2023	C587196
H2323107	Certificate of Analysis	Aug 03, 2023	C587196
H2323108	Certificate of Analysis	Aug 03, 2023	C587196
H2323105	Certificate of Analysis	Aug 03, 2023	C587196

Chemical and Physical Properties

Sensitivity	air sensitive；heat sensitive
Melt Point(°C)	204 °C
Molecular Weight	388.200 g/mol
XLogP3
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	3
Exact Mass	387.039 Da
Monoisotopic Mass	387.039 Da
Topological Polar Surface Area	141.000 Å²
Heavy Atom Count	25
Formal Charge	0
Complexity	414.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	2

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