Chloramphenicol 1-Acetate - ≥98% , CAS No.23214-93-9

CAS: 23214-93-9 Cat. No.: C348072 Peso molecular: 365.17

GRADE & PURITY ≥98%

Synonyms

Acetamide, N-[(1R,2R)-2-(acetyloxy)-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl]-2,2-dichloro- | Acetylchloramphenicol, 1- | Acetamide, N-(2-(acetyloxy)-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl)-2,2-dichloro-, (R-(R*,R*))- | 1-Acetylchloramphenicol | Chloram

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general

Found in the metabolic decomposition of Chloramphenicol by Alcaligenes faecalis. A Chloramphenicol derivative.

Specifications

Sinónimos

Acetamide, N-[(1R, 2R)-2-(acetyloxy)-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl]-2, 2-dichloro- | Acetylchloramphenicol, 1- | Acetamide, N-(2-(acetyloxy)-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl)-2, 2-dichloro-, (R-(R*, R*))- | 1-Acetylchloramphenicol | Chloram

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504755736
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755736
• Sonrisas canónicas: CC(=O)OC(C1=CC=C(C=C1)[N+](=O)[O-])C(CO)NC(=O)C(Cl)Cl
• IUPAC Name: [(1R,2R)-2-[(2,2-dichloroacetyl)amino]-3-hydroxy-1-(4-nitrophenyl)propyl] acetate
• InChIKey: WEYAPUCXWINQDH-GHMZBOCLSA-N
• INCHI: 1S/C13H14Cl2N2O6/c1-7(19)23-11(10(6-18)16-13(20)12(14)15)8-2-4-9(5-3-8)17(21)22/h2-5,10-12,18H,6H2,1H3,(H,16,20)/t10-,11-/m1/s1
• Isómeros SMILES: CC(=O)O[C@H](C1=CC=C(C=C1)[N+](=O)[O-])[C@@H](CO)NC(=O)C(Cl)Cl
• Peso molecular: 365.17
• Reaxy-Rn: 2911434
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2911434&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Benzyloxycarbonyls

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Benzyloxycarbonyls
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzyloxycarbonyls
• Alternative Parents: Nitrobenzenes Nitroaromatic compounds Secondary carboxylic acid amides Carboxylic acid esters Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Organic oxoazanium compounds Alkyl chlorides Organic oxides Organopnictogen compounds Primary alcohols Carbonyl compounds Hydrocarbon derivatives Organic zwitterions Organochlorides Organonitrogen compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzyloxycarbonyl - Nitrobenzene - Nitroaromatic compound - Carboxamide group - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organochloride - Alkyl halide - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Alkyl chloride - Organopnictogen compound - Alcohol - Organic oxygen compound - Organooxygen compound - Primary alcohol - Organic zwitterion - Organic nitrogen compound - Carbonyl group - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as benzyloxycarbonyls. These are organic compounds containing a carbonyl group substituted with a benzyloxyl group.
• External Descriptors: Not available

Data sources

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

Objetivos asociados (no humanos)

Mycobacterium tuberculosis (203094 Activities)

Explore this target

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Chloroform (Slightly), Ethyl Acetate, Methanol (Slightly)
• Punto de fusión (°C): >119° C (dec.)
• Peso molecular: 365.160 g/mol
• XLogP3: 1.700
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• Exact Mass: 364.023 Da
• Monoisotopic Mass: 364.023 Da
• Topological Polar Surface Area: 121.000 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 435.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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