Allylmagnesium chloride solution - 2.0 M in THF, used for Allylmagnesium chloride solution is used as a Grignard reagent in the preparation of: Antipsychotic clopixol. Polysilane–crown ether polymer (PSEC) using hexachloroplatinic acid as a catalyst. 1,7-

CAS: 2622-05-1 Cat. No.: A432500 Fórmula: C₃H₅ClMg Peso molecular: 100.83 Beilstein Registry Number: 3587316 Número CE: 220-067-1

GRADE & PURITY 2.0 M in THF

Storage

Room temperature

Shipped In

Normal

Visão geral

Allylmagnesiumchloride solution is an organic compound commonly used as a Grignard reagent inchemical reactions. It is used for the allylation of carbonyl compounds, such as aldehydes and ketones.

Specifications

Especificações e pureza

2.0 M in THF

Aplicação

Allylmagnesium chloride solution is used as a Grignard reagent in the preparation of: Antipsychotic clopixol. Polysilane–crown ether polymer (PSEC) using hexachloroplatinic acid as a catalyst. 1,7-disubstituted-1,2,3,4-tetrahydroisoquinolinesfrom 3,4-dihy

Condições de armazenamento de armazenamento

Room temperature

Enviado em

Normal

Nomes e identificadores

• Sorrisos canónicos: [CH2-]C=C.[Mg+2].[Cl-]
• IUPAC Name: magnesium;prop-1-ene;chloride
• InChIKey: CYSFUFRXDOAOMP-UHFFFAOYSA-M
• INCHI: 1S/C3H5.ClH.Mg/c1-3-2;;/h3H,1-2H2;1H;/q-1;;+2/p-1
• SMILES isoméricas: [CH2-]C=C.[Mg+2].[Cl-]
• WGK Alemanha: 1
• Número UN: 3399
• Grupo de embalagem: I
• Peso molecular: 100.83
• Beilstein: 3587316
• Reaxy-Rn: 3587316
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3587316&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic salts
    • Classe Organic metal salts
      • Subclass Organic metal halides

• Kingdom: Organic compounds
• Superclass: Organic salts
• Classe: Organic metal salts
• Subclass: Organic metal halides
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic metal halides
• Alternative Parents: Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic metal halide - Hydrocarbon derivative - Organic chloride salt - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as organic metal halides. These are organic compounds containing metals and halogens. Some are ionic while others are covalently bonded.
• 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

Propriedades químicas e físicas

• Ponto de inflamação (°F): 1.4 °F
• Ponto de inflamação (°C): -17°C
• Ponto de ebulição (°C): 66°C
• Ponto de fusão (°C): -21°C
• Peso molecular: 100.830 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 99.993 Da
• Monoisotopic Mass: 99.993 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 14.400
• 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: 3

XLogP3

Referências

1. Zhensheng Huang, Jingang Zhang, Biao Jiang, Lu Zhou.  (2025)  Synthesis of a gemini fluorinated sulfonate surfactant and its synergy with nano-SiO₂.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.139004]