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612086-27-8

Pyridine, 4-chloro-3-(2-phenyl-1-naphthalenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 612086-27-8 Structure

  • Basic information

    1. Product Name: Pyridine, 4-chloro-3-(2-phenyl-1-naphthalenyl)-
    2. Synonyms:
    3. CAS NO:612086-27-8
    4. Molecular Formula: C21H14ClN
    5. Molecular Weight: 315.802
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 612086-27-8.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: Pyridine, 4-chloro-3-(2-phenyl-1-naphthalenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyridine, 4-chloro-3-(2-phenyl-1-naphthalenyl)-(612086-27-8)
    11. EPA Substance Registry System: Pyridine, 4-chloro-3-(2-phenyl-1-naphthalenyl)-(612086-27-8)

  • 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: 612086-27-8(Hazardous Substances Data)

612086-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 612086-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,2,0,8 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 612086-27:
(8*6)+(7*1)+(6*2)+(5*0)+(4*8)+(3*6)+(2*2)+(1*7)=128
128 % 10 = 8
So 612086-27-8 is a valid CAS Registry Number.

612086-27-8Relevant articles and documents

Preparative-Scale Synthesis of Vedejs Chiral DMAP Catalysts

Kinens, Artis,Balkaitis, Simonas,Suna, Edgars

, p. 12449 - 12459 (2018/10/20)

A scalable synthesis of chiral Vedejs-type DMAP catalysts is reported. The key step of the synthesis is amination of the enantiomerically pure 4-chloropyridine derivative using well-defined ZnCl2(amine)2 complexes. A series of Zn(II)-amine complexes have been synthesized to explore the scope of the ZnCl2-mediated amination of 4-halopyridines. Mechanistic studies support a Zn(II)-facilitated nucleophilic aromatic substitution as a plausible mechanism for the chlorine-to-amine exchange.

PROCESS FOR THE PREPARATION OF ATROPISOMERIC ANALOGUES OF 4-AMINOPYRIDINE

-

Page 13; 14, (2010/02/10)

The present invention relates to a process for the preparation of 3,4-disubstituted pyridines from commercially available starting materials. In particular, the invention relates to the process for the preparation for a compound of formula (I) wherein a c

Concise synthesis, preparative resolution, absolute configuration determination, and applications of an atropisomeric biaryl catalyst for asymmetric acylation

Spivey, Alan C.,Zhu, Fujiang,Mitchell, Mark B.,Davey, Stephen G.,Jarvest, Richard L.

, p. 7379 - 7385 (2007/10/03)

A new three-step synthesis and resolution of nucleophilic catalyst 1 suitable for large-scale preparation has been developed, and this catalyst has been shown to be effective for the kinetic resolution and asymmetric desymmetrization of a range of sec-alcohol substrates.

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