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3,5-dimethyl-2,6-diphenylpiperidin-4-ol is a complex organic compound belonging to the piperidine family, characterized by a six-membered nitrogen-containing ring structure. This specific compound features two methyl groups at the 3rd and 5th positions, and two phenyl groups at the 2nd and 6th positions, with a hydroxyl group attached at the 4th position. It is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs and medicinal compounds. The compound's unique structure and functional groups contribute to its diverse chemical properties and reactivity, making it a subject of interest for researchers in organic chemistry and drug development.

2403-94-3

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2403-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2403-94-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2403-94:
(6*2)+(5*4)+(4*0)+(3*3)+(2*9)+(1*4)=63
63 % 10 = 3
So 2403-94-3 is a valid CAS Registry Number.

2403-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-2,6-diphenylpiperidin-4-ol

1.2 Other means of identification

Product number -
Other names cis-3,5-Dimethyl-2,6-diphenylpiperidin-4-ol

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:2403-94-3 SDS

2403-94-3Relevant academic research and scientific papers

Design, synthesis, molecular docking and antimicrobial evaluation of some tosyl carbamate derivatives

Kalaivani, Panneerselvam,Arikrishnan, Jayaraman,Gopalakrishnan, Mannuthusamy

, p. 783 - 788 (2020/03/24)

A series of tosyl carbamates have been synthesized and screened for their antibacterial and antifungal activities. All the synthesized compounds were characterized by spectral techniques (IR, 1H, 13C NMR and mass) and elemental analysis. in silico Molecular docking method was performed to study their antimicrobial activity against the target protein 1T9U. Compound 27 showed good antibacterial activity against Gram-positive and Gram-negative bacterial strains and compound 19 showed good antifungal activity. Molecular docking results revealed that the compound 19 exhibits minimum CDOCKER energy. Tosyl carbamate derivatives having good antimicrobial activities compared to that standard and all the synthesized compounds exhibits moderate CDOCKER scores.

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