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1017601-63-6

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1017601-63-6 Usage

Chemical class

Pyridinones

Type of compound

Heterocyclic

Structural components

Nitrogen-containing six-membered ring, benzyl group, chlorophenyl group, pyridinone ring

Pharmacological properties

Potential (due to structure)

Safety precautions

Potential toxicity and reactivity

Uses

Intermediate in the synthesis of pharmaceuticals or other organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 1017601-63-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,6,0 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1017601-63:
(9*1)+(8*0)+(7*1)+(6*7)+(5*6)+(4*0)+(3*1)+(2*6)+(1*3)=106
106 % 10 = 6
So 1017601-63-6 is a valid CAS Registry Number.

1017601-63-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-5-(4-chlorophenyl)-2,3-dihydropyridin-4-one

1.2 Other means of identification

Product number -
Other names 1-benzyl-5-(4-chlorophenyl)-2,3-dihydropyridin-4(1H)-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1017601-63-6 SDS

1017601-63-6Downstream Products

1017601-63-6Relevant articles and documents

Palladium(II)-catalyzed direct arylation of enaminones using organotrifluoroborates

Ge, Haibo,Niphakis, Micah J.,Georg, Gunda I.

, p. 3708 - 3709 (2008/09/21)

A Pd(II)-catalyzed reaction for the direct arylation of cyclic enaminones is reported. The reactivity of electron-rich, electron-poor, and sterically encumbered organotrifluoroborates was investigated. This reaction represents a unique use for organotrifluoroborates as coupling partners and discloses the utility of enaminones for direct-functionalization reactions. It provides immediate access to arylpiperidine, indolizidine, and quinolizidine scaffolds from the corresponding mono- and bicyclic, unattenuated enaminones. Copyright

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