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3-phenyl-o-carborane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65600-05-7 Structure
  • Basic information

    1. Product Name: 3-phenyl-o-carborane
    2. Synonyms: 3-phenyl-o-carborane
    3. CAS NO:65600-05-7
    4. Molecular Formula:
    5. Molecular Weight: 220.325
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65600-05-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-phenyl-o-carborane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-phenyl-o-carborane(65600-05-7)
    11. EPA Substance Registry System: 3-phenyl-o-carborane(65600-05-7)
  • 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: 65600-05-7(Hazardous Substances Data)

65600-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65600-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,0 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65600-05:
(7*6)+(6*5)+(5*6)+(4*0)+(3*0)+(2*0)+(1*5)=107
107 % 10 = 7
So 65600-05-7 is a valid CAS Registry Number.

65600-05-7Downstream Products

65600-05-7Relevant articles and documents

Ir-Catalyzed Selective B(3)-H Amination of o-Carboranes with NH3

Au, Yik Ki,Zhang, Jie,Quan, Yangjian,Xie, Zuowei

, p. 4148 - 4153 (2021)

Ammonia gas, NH3, is a cheap and widely used industrial feedstock, which has received tremendous research interests in its functionalization. This work reports a breakthrough in catalytic selective cage B(3)-H amination of o-carboranes with NH3 via Ir-catalyzed B-H/N-H dehydrocoupling, offering convenient and efficient access to a series of 3-NH2-o-carborane derivatives in moderate to high isolated yields with a broad substrate scope. The employment of readily available NH3 gas as the aminating reagent with H2 as the sole byproduct endows the protocol economy, practicability, and environmental friendliness. A plausible reaction mechanism is proposed on the basis of control experiments.

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