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[RH (COD) (-) TETRAME-BITIOP] BF4 is a complex chemical compound that consists of the metal rhodium, the ligand tetrakis(tetramethylphosphonium) tetrathiotungstate, and the counterion tetrafluoroborate. It is known for its high catalytic activity and selectivity in various chemical reactions, making it a valuable tool in the field of organic synthesis and coordination chemistry.

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  • 266316-99-8 Structure
  • Basic information

    1. Product Name: [RH (COD) (-) - TETRAME-BITIOP] BF4
    2. Synonyms: [RH (COD) (-) - TETRAME-BITIOP] BF4
    3. CAS NO:266316-99-8
    4. Molecular Formula: MW:
    5. Molecular Weight: 886.6
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 266316-99-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: [RH (COD) (-) - TETRAME-BITIOP] BF4(CAS DataBase Reference)
    10. NIST Chemistry Reference: [RH (COD) (-) - TETRAME-BITIOP] BF4(266316-99-8)
    11. EPA Substance Registry System: [RH (COD) (-) - TETRAME-BITIOP] BF4(266316-99-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 266316-99-8(Hazardous Substances Data)

266316-99-8 Usage

Uses

Used in Organic Synthesis:
[RH (COD) (-) TETRAME-BITIOP] BF4 is used as a catalyst for enhancing the efficiency and selectivity of various chemical reactions in the field of organic synthesis. Its unique properties allow chemists and researchers to develop new pharmaceuticals, materials, and other important chemical products.
Used in Coordination Chemistry Research:
[RH (COD) (-) TETRAME-BITIOP] BF4 is also used as a subject of study in the field of coordination chemistry due to its interesting properties. This helps researchers gain a deeper understanding of the compound's behavior and potential applications in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 266316-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,6,3,1 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 266316-99:
(8*2)+(7*6)+(6*6)+(5*3)+(4*1)+(3*6)+(2*9)+(1*9)=158
158 % 10 = 8
So 266316-99-8 is a valid CAS Registry Number.

266316-99-8Downstream Products

266316-99-8Relevant articles and documents

Process-scale total synthesis of nature-identical (-)-(S,S)-7- hydroxycalamenal in high enantiomeric purity through catalytic enantioselective hydrogenation

Benincori, Tiziana,Bruno, Silvana,Celentano, Giuseppe,Pilati, Tullio,Ponti, Alessandro,Rizzo, Simona,Sada, Mara,Sannicolo, Francesco

, p. 1776 - 1789 (2007/10/03)

A process-scale stereoselective synthesis of nature-identical (-)-(S,S)-7-hydroxycalamenal (=(-)-(5S,85)-5,6,7,8-tetrahydro-3-hydroxy-5- methyl-8-(1-methylethyl)naphthalene-2-carbaldehyde; (-)-1α) in 96% enantiomeric excess (ee) with the aid of chiral Ru

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