Taxonomic Classification

Taxonomy Tree

Kingdom	Organic compounds
Superclass	Benzenoids
Clase	Benzene and substituted derivatives
Subclass	Benzoic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Benzamides
Alternative Parents	Phenoxy compounds Phenol ethers Benzoyl derivatives Alkyl aryl ethers Primary carboxylic acid amides Dialkyl ethers Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Benzamide - Phenoxy compound - Benzoyl - Phenol ether - Alkyl aryl ether - Carboxamide group - Primary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Ether - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
Descripción	This compound belongs to the class of organic compounds known as benzamides. These are organic compounds containing a carboxamido substituent attached to a benzene ring.
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

Estructura 3D

Objetivos asociados (no humanos)

Hdac6 Histone deacetylase 6 (222 Activities)

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

rep Replicase polyprotein 1ab (378 Activities)

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

Mecanismos de acción

Certificados (CoA, COO, BSE/TSE y tabla de análisis)

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	Fecha	Articulo
I2207631	Certificate of Analysis	Jun 16, 2025	E413641
I2207630	Certificate of Analysis	Jun 16, 2025	E413641
I2207629	Certificate of Analysis	Jun 16, 2025	E413641
C2527104	Certificate of Analysis	Jun 24, 2022	E413641

Propiedades químicas y físicas

Solubilidad	Solubility (25°C) In vitro DMSO: 42 mg/mL (200.72 mM); Ethanol: 42 mg/mL (200.72 mM); Water: 6 mg/mL (28.67 mM);
Sensibilidad	light sensitive
DMSO (mg/ml) Solubilidad máxima	42
DMSO (mM) Solubilidad máxima	200.726438539476
Agua (mg/ml) Solubilidad máxima	6
Agua (mM) Solubilidad máxima	28.6752055056395
Peso molecular	209.240 g/mol
XLogP3	1.100
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	6
Exact Mass	209.105 Da
Monoisotopic Mass	209.105 Da
Topological Polar Surface Area	61.600 Å²
Heavy Atom Count	15
Formal Charge	0
Complexity	196.000
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	1

Calculadoras de soluciones

Determine the necessary mass, volume, or concentration for preparing a solution.

Determine the dilution needed to prepare a stock solution.

Reseñas

Pubchem Sid	504757841
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504757841
Sonrisas canónicas	CCOCCOC1=CC=CC=C1C(=O)N
IUPAC Name	2-(2-ethoxyethoxy)benzamide
InChIKey	XBNRCMFFZFCWMH-UHFFFAOYSA-N
INCHI	1S/C11H15NO3/c1-2-14-7-8-15-10-6-4-3-5-9(10)11(12)13/h3-6H,2,7-8H2,1H3,(H2,12,13)
Isómeros SMILES	CCOCCOC1=CC=CC=C1C(=O)N
Peso molecular	209.24
Reaxy-Rn	2646194
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2646194&ln=

Etosalamide - ≥98% , CAS No.15302-15-5

Descripción general