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192189-63-2

6-Bromo-1-(tert-butyl-diphenyl-silanyl)-3-methyl-4-propyl-1H-pyridin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 192189-63-2 Structure

  • Basic information

    1. Product Name: 6-Bromo-1-(tert-butyl-diphenyl-silanyl)-3-methyl-4-propyl-1H-pyridin-2-one
    2. Synonyms: 6-Bromo-1-(tert-butyl-diphenyl-silanyl)-3-methyl-4-propyl-1H-pyridin-2-one
    3. CAS NO:192189-63-2
    4. Molecular Formula:
    5. Molecular Weight: 468.509
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 192189-63-2.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: 6-Bromo-1-(tert-butyl-diphenyl-silanyl)-3-methyl-4-propyl-1H-pyridin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Bromo-1-(tert-butyl-diphenyl-silanyl)-3-methyl-4-propyl-1H-pyridin-2-one(192189-63-2)
    11. EPA Substance Registry System: 6-Bromo-1-(tert-butyl-diphenyl-silanyl)-3-methyl-4-propyl-1H-pyridin-2-one(192189-63-2)

  • 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: 192189-63-2(Hazardous Substances Data)

192189-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192189-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,1,8 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 192189-63:
(8*1)+(7*9)+(6*2)+(5*1)+(4*8)+(3*9)+(2*6)+(1*3)=162
162 % 10 = 2
So 192189-63-2 is a valid CAS Registry Number.

192189-63-2Relevant articles and documents

Synthesis of (S)-Mappicine and mappicine ketone via radical cascade reaction of isonitriles

Josien, Hubert,Curran, Dennis P.

, p. 8881 - 8886 (1997)

(S)-Mappicine (2) and mappicine ketone (1) have been prepared from methylacetoacetate (4) by a strategy featuring a radical cascade reaction of an isonitrile as the key step. The introduction of the hydroxy group of (S)- mappicine occurred with moderate selectivity through asymmetric hydroxylation.

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