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(1-phenylsulfonyl-3-indolyl)-2-naphthylmethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1008533-23-0 Structure
  • Basic information

    1. Product Name: (1-phenylsulfonyl-3-indolyl)-2-naphthylmethanol
    2. Synonyms: (1-phenylsulfonyl-3-indolyl)-2-naphthylmethanol
    3. CAS NO:1008533-23-0
    4. Molecular Formula:
    5. Molecular Weight: 413.497
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1008533-23-0.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: (1-phenylsulfonyl-3-indolyl)-2-naphthylmethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1-phenylsulfonyl-3-indolyl)-2-naphthylmethanol(1008533-23-0)
    11. EPA Substance Registry System: (1-phenylsulfonyl-3-indolyl)-2-naphthylmethanol(1008533-23-0)
  • 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: 1008533-23-0(Hazardous Substances Data)

1008533-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1008533-23-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,5,3 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1008533-23:
(9*1)+(8*0)+(7*0)+(6*8)+(5*5)+(4*3)+(3*3)+(2*2)+(1*3)=110
110 % 10 = 0
So 1008533-23-0 is a valid CAS Registry Number.

1008533-23-0Downstream Products

1008533-23-0Relevant articles and documents

Efficient 1,2-addition of aryl- and alkenylboronic acids to aldehydes catalyzed by the palladium/thioether-imidazolinium chloride system

Kuriyama, Masami,Shimazawa, Rumiko,Shirai, Ryuichi

, p. 1597 - 1600 (2008)

(Chemical Equation Presented) The high level of catalyst performance was attainable in the palladium-catalyzed 1,2-addition of aryl-, heteroaryl-, and alkenylboronic acids to aromatic, heteroaromatic, and aliphatic aldehydes using thioether-imidazolinium chloride L5 as a heterobidentate carbene ligand precursor.

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