Cloruro de Fmoc - para derivatización HPLC, ≥99%(HPLC) , CAS No.28920-43-6

CAS: 28920-43-6 Cat. No.: F106534 Peso molecular: 258.7 Beilstein Registry Number: 2279177 Número EC: 249-313-6

GRADE & PURITY for HPLC derivatization, ≥99%(HPLC)

Synonyms

Fmoc-Cl | Cloruro de (9H-Fluoren-9-ilmetoxi)carbonilo | Cloruro de 9-Fluorenilmetoxicarbonilo | Cloroformato de 9-Fluorenilmetilo | Ácido Cloroformico 9-Fluorenilmetilo Ester

Storage

Conservar a 2-8°C,Cargado con argón,Desecado

Shipped In

Hielo húmedo

Descripción general

Agente derivatizante de aminoácidos para el análisis de HLPC. Reactivo N-protector para síntesis de péptidos y oligonucleótidos. Reactivo para la protección de grupos amino utilizado recientemente en la síntesis de un análogo bicíclico de la prolina. Reactivo para la derivatización de aminoácidos para el análisis de aminoácidos por HPLC y para la preparación de aminoácidos N-Fmoc para la síntesis de péptidos en fase sólida.

Specifications

Sinónimos

Fmoc-Cl | Cloruro de (9H-Fluoren-9-ilmetoxi)carbonilo | Cloruro de 9-Fluorenilmetoxicarbonilo | Cloroformato de 9-Fluorenilmetilo | Ácido Cloroformico 9-Fluorenilmetilo Ester

Especificaciones y pureza

para derivatización HPLC, ≥99%(HPLC)

Condiciones de almacenamiento de almacenamiento

Conservar a 2-8°C, Cargado con argón, Desecado

Enviado en

Hielo húmedo

Grado

for HPLC derivatization

Pureza

≥99%(HPLC)

Nombres e identificadores

• Sonrisas canónicas: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)Cl
• IUPAC Name: 9H-fluoren-9-ylmethyl carbonochloridate
• InChIKey: IRXSLJNXXZKURP-UHFFFAOYSA-N
• INCHI: 1S/C15H11ClO2/c16-15(17)18-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2
• Isómeros SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)Cl
• WGK Alemania: 3
• RTECS: LQ6250000
• Número ONU: 3261
• Peso molecular: 258.7
• Beilstein: 2279177
• Reaxy-Rn: 2279177
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2279177&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Fluorenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Fluorenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorenes
• Alternative Parents: Organic carbonic acids and derivatives Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Fluorene - Carbonic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Carbonyl group - Aromatic homopolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as fluorenes. These are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene.
• 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

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive;Heat sensitive
• Punto de fusión (°C): 61.0 - 65.0 °C
• Peso molecular: 258.700 g/mol
• XLogP3: 4.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 258.045 Da
• Monoisotopic Mass: 258.045 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 296.000
• 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

Referencias

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