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870843-42-8

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  • 2-Piperidinone,1-[(1S)-1-(4-fluorophenyl)ethyl]-3-[[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]methylene]-,(3E)-

    Cas No: 870843-42-8

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  • (E)-1-[(1S)-1-(4-Fluorophenyl)ethyl]-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene]piperidin-2-one

    Cas No: 870843-42-8

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  • 2-Piperidinone,1-[(1S)-1-(4-fluorophenyl)ethyl]-3-[[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]methylene]-,(3E)-

    Cas No: 870843-42-8

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870843-42-8 Usage

General Description

The chemical compound "(E)-1-[(1S)-1-(4-Fluorophenyl)ethyl]-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene]piperidin-2-one" is a complex molecule with a piperidin-2-one core structure and multiple functional groups. It contains a fluorophenyl group, a methoxybenzylidene group, and an imidazol-1-yl group, among others. (E)-1-[(1S)-1-(4-Fluorophenyl)ethyl]-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene]piperidin-2-one has potential pharmaceutical applications due to its structural features, which could contribute to its interactions with biological targets. This chemical may have activities related to the central nervous system, as piperidin-2-one derivatives are known for their neurological effects. Further studies on its pharmacological properties and potential therapeutic uses could reveal interesting applications for this compound in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 870843-42-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,8,4 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 870843-42:
(8*8)+(7*7)+(6*0)+(5*8)+(4*4)+(3*3)+(2*4)+(1*2)=188
188 % 10 = 8
So 870843-42-8 is a valid CAS Registry Number.
InChI:InChI=1/C25H26FN3O2/c1-17-15-28(16-27-17)23-11-6-19(14-24(23)31-3)13-21-5-4-12-29(25(21)30)18(2)20-7-9-22(26)10-8-20/h6-11,13-16,18H,4-5,12H2,1-3H3/b21-13+/t18-/m0/s1

870843-42-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3E)-1-[(1S)-1-(4-fluorophenyl)ethyl]-3-[[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]methylidene]piperidin-2-one

1.2 Other means of identification

Product number -
Other names (S,E)-1-(1-(4-fluorophenyl)ethyl)-3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene)piperidin-2-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

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More Details:870843-42-8 SDS

870843-42-8Relevant articles and documents

ONE-POT METHODS FOR PREPARING CINNAMIDE DERIVATIVES

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Page/Page column 8; 9, (2009/01/24)

A compound represented by the following formula (1): wherein R represents a 4-fluorophenyl group and the like; Q represents —CH(CH3)— and the like; and n represents 1 and the like and a pharmaceutically acceptable salt thereof can be prepared in one-pot by reacting a compound represented by the following formula (2): wherein R1 represents a 4-fluorophenyl group and the like; and Q and n have the same meaning as described above, with 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde in the presence of a base and, if necessary, removing a protecting group.

PROCESS FOR PRODUCTION OF CINNAMAMIDE DERIVATIVE

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Page/Page column 52-53, (2008/12/07)

A compound (8) represented by the formula: (8) wherein R1 represents a 6- to 14-membered aromatic hydrocarbon ring group which may have a substituent; and n represents 0 to 2, can be produced with good efficiency by reacting a compound (3) represented by the formula: (3) wherein R1 and n are as defined above; and Q represents a single bond or -CH(Y)- where Y represents a hydrogen atom or a C1-6 alkyl group] with 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde in the presence of a base.

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