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1027913-81-0

1-(1-benzhydryl-1,4-dihydro-pyridin-3-yl)-ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1027913-81-0 Structure

  • Basic information

    1. Product Name: 1-(1-benzhydryl-1,4-dihydro-pyridin-3-yl)-ethanone
    2. Synonyms:
    3. CAS NO:1027913-81-0
    4. Molecular Formula:
    5. Molecular Weight: 289.377
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1027913-81-0.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-(1-benzhydryl-1,4-dihydro-pyridin-3-yl)-ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(1-benzhydryl-1,4-dihydro-pyridin-3-yl)-ethanone(1027913-81-0)
    11. EPA Substance Registry System: 1-(1-benzhydryl-1,4-dihydro-pyridin-3-yl)-ethanone(1027913-81-0)

  • 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: 1027913-81-0(Hazardous Substances Data)

1027913-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1027913-81-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,9,1 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1027913-81:
(9*1)+(8*0)+(7*2)+(6*7)+(5*9)+(4*1)+(3*3)+(2*8)+(1*1)=140
140 % 10 = 0
So 1027913-81-0 is a valid CAS Registry Number.

1027913-81-0Upstream product

1027913-81-0Relevant articles and documents

A synthetic entry to 3,5-disubstituted pyridines

Bennasar, M.-Llu?sa,Zulaica, Ester,Roca, Tomàs,Alonso, Yolanda,Monerris, Manuel

, p. 4711 - 4714 (2003)

A straightforward entry to 3,5-disubstituted pyridines from 3-substituted pyridines, based on the acylation of N-alkyl-1,4-dihydropyridine derivatives followed by a tandem N-dealkylation-oxidation sequence is reported.

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