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Catalog Number:
35982
CAS Number:
804482-50-6
Cloruro de (3,3,3-tricloropropil)trifenilfosfonio
Purity:
≥ 95% (Ensayo por titulación)
Synonym(s):
Cloruro de trifenil(3,3,3-tricloropropil)fosfonio
Documents
$162.00 /1G
Tamaño
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Product Information

Se utiliza como reactivo para la síntesis de DL-histrionicotoxina a través de una síntesis de nueve pasos que implica metátesis cruzada, formación de oxima y adición de Michael como pasos clave.

Synonyms
Cloruro de trifenil(3,3,3-tricloropropil)fosfonio
CAS Number
804482-50-6
Purity
≥ 95% (Ensayo por titulación)
Molecular Formula
C21H19Cl4P
Molecular Weight
444.16
MDL Number
MFCD09265083
PubChem ID
11751136
Melting Point
138 - 145 ?C
Appearance
Polvo cristalino blanco
Conditions
Tienda en RT
General Information
Synonyms
Cloruro de trifenil(3,3,3-tricloropropil)fosfonio
CAS Number
804482-50-6
Purity
≥ 95% (Ensayo por titulación)
Molecular Formula
C21H19Cl4P
Molecular Weight
444.16
MDL Number
MFCD09265083
PubChem ID
11751136
Melting Point
138 - 145 ?C
Appearance
Polvo cristalino blanco
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(3,3,3-Trichloropropyl)triphenylphosphonium chloride is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the synthesis of various complex molecules. Its ability to introduce the trichloropropyl group can enhance the reactivity of substrates.
  • Pharmaceutical Development: It is used in the pharmaceutical industry to create intermediates for drug compounds, particularly those targeting specific biological pathways, improving the efficiency of drug discovery.
  • Material Science: The compound finds applications in the development of new materials, including polymers and coatings, where its unique properties can enhance material performance and durability.
  • Biochemical Research: Researchers utilize it in biochemical studies to investigate cellular processes, particularly in studies involving membrane interactions and cellular transport mechanisms.
  • Agricultural Chemistry: It is also explored in the formulation of agrochemicals, where it can contribute to the development of more effective pesticides or herbicides, improving crop protection strategies.

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