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CAS

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1024585-97-4

2-(4'-tert-butyl-3,4,5,6-tetradeuteriobiphenyl-2-yl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1024585-97-4 Structure

  • Basic information

    1. Product Name: 2-(4'-tert-butyl-3,4,5,6-tetradeuteriobiphenyl-2-yl)pyridine
    2. Synonyms: 2-(4'-tert-butyl-3,4,5,6-tetradeuteriobiphenyl-2-yl)pyridine
    3. CAS NO:1024585-97-4
    4. Molecular Formula:
    5. Molecular Weight: 291.373
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1024585-97-4.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: 2-(4'-tert-butyl-3,4,5,6-tetradeuteriobiphenyl-2-yl)pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4'-tert-butyl-3,4,5,6-tetradeuteriobiphenyl-2-yl)pyridine(1024585-97-4)
    11. EPA Substance Registry System: 2-(4'-tert-butyl-3,4,5,6-tetradeuteriobiphenyl-2-yl)pyridine(1024585-97-4)

  • 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: 1024585-97-4(Hazardous Substances Data)

1024585-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1024585-97-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,4,5,8 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1024585-97:
(9*1)+(8*0)+(7*2)+(6*4)+(5*5)+(4*8)+(3*5)+(2*9)+(1*7)=144
144 % 10 = 4
So 1024585-97-4 is a valid CAS Registry Number.

1024585-97-4Downstream Products

1024585-97-4Relevant articles and documents

Iron-catalyzed direct arylation through directed C-H bond activation

Norinder, Jakob,Matsumoto, Arimasa,Yoshikai, Naohiko,Nakamura, Eiichi

, p. 5858 - 5859 (2008)

An iron-catalyzed C-C bond formation reaction of a nitrogen-containing aromatic compound with an arylzinc reagent takes place at 0 °C in a good to quantitative yield. The reaction involves a C-H bond activation directed by a neighboring nitrogen atom. The important additives in this reaction are 1,10-phenanthroline, tetramethylethylenediamine, and 1,2-dichloro-2-methylpropane, in the absence of which a very low product yield was observed. Copyright

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