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97112-11-3

1,5-Diphenyl-5,6,7,8-tetrahydro-isoquinolin-5-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97112-11-3 Structure

  • Basic information

    1. Product Name: 1,5-Diphenyl-5,6,7,8-tetrahydro-isoquinolin-5-ol
    2. Synonyms:
    3. CAS NO:97112-11-3
    4. Molecular Formula:
    5. Molecular Weight: 301.388
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97112-11-3.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: 1,5-Diphenyl-5,6,7,8-tetrahydro-isoquinolin-5-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,5-Diphenyl-5,6,7,8-tetrahydro-isoquinolin-5-ol(97112-11-3)
    11. EPA Substance Registry System: 1,5-Diphenyl-5,6,7,8-tetrahydro-isoquinolin-5-ol(97112-11-3)

  • 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: 97112-11-3(Hazardous Substances Data)

97112-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97112-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,1,1 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97112-11:
(7*9)+(6*7)+(5*1)+(4*1)+(3*2)+(2*1)+(1*1)=123
123 % 10 = 3
So 97112-11-3 is a valid CAS Registry Number.

97112-11-3Downstream Products

97112-11-3Relevant articles and documents

Applications of Organolithium and Related Reagents in Synthesis. Part 3. A General Study of the Reaction of Lithium Alkyls with Pyridine Ketones

Epsztajn, Jan,Bieniek, Adam

, p. 213 - 220 (2007/10/02)

The reaction of MeLi and PhLi with acetylpyridines (1a-c) and their annelated derivatives (2a), (2b), (3), and (4) has been examined.The 3- and 4-pyridyl ketones (1b), (1c), (3), and (4) gave similar results to acetophenone and 3,4-dihydronaphthalen-1(2H)-one.In the case of the 2-pyridyl ketones (1a), (2a), and (2b) unexpectedly low yields of products resulted from the addition of RLi to the carbonyl group; the reaction was efficiently enhanced by initially adding an additional amount of LiBr.These results were accounted for by the chelation of RLi or LiBr by the 2-pyridyl ketones.

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