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26822-37-7

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26822-37-7 Usage

General Description

PIPERIDINIUM, 1,1-DIMETHYL-4-OXO-, IODIDE is a chemical compound with the molecular formula C7H14NOI. It is a quaternary ammonium salt with a piperidine ring substituted with a 1,1-dimethyl-4-oxo group and an iodide ion. It is commonly used in organic synthesis as a phase-transfer catalyst, which facilitates the transfer of reactants between immiscible phases during chemical reactions. PIPERIDINIUM, 1,1-DIMETHYL-4-OXO-, IODIDE has potential application in the pharmaceutical industry and in the production of various organic compounds. Its properties and reactivity make it a versatile and valuable chemical in organic chemistry research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 26822-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,8,2 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26822-37:
(7*2)+(6*6)+(5*8)+(4*2)+(3*2)+(2*3)+(1*7)=117
117 % 10 = 7
So 26822-37-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H14NO/c1-8(2)5-3-7(9)4-6-8/h3-6H2,1-2H3/q+1

26822-37-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dimethylpiperidin-1-ium-4-one,iodide

1.2 Other means of identification

Product number -
Other names N-Methyl-4-piperidone methodide

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:26822-37-7 SDS

26822-37-7Relevant articles and documents

SUBSTITUTED 3-((3-AMINOPHENYL)AMINO)PIPERIDINE-2,6-DIONE COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH

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Paragraph 0519; 0520, (2020/07/14)

Provided herein are piperidine dione compounds having the following structure: wherein RN, R1, R2, R3, R4, X, L, V, m, and n are as defined herein, compositions comprising an effective amount of a piperidine dione compound, and methods for treating or preventing an androgen receptor mediated disease.

Synthesis and Antimicrobial Evaluation of Novel Chiral 2-Amino-4,5,6,7-tetrahydrothieno[2,3-c]pyridine Derivatives

Rossetti, Arianna,Bono, Nina,Candiani, Gabriele,Meneghetti, Fiorella,Roda, Gabriella,Sacchetti, Alessandro

, (2019/05/15)

New N-substituted-2-amino-4,5,6,7-tetrahydrothieno[2,3-c]pyridine derivatives were synthesized employing a convenient one-pot three-component method and their structures were characterized by 1H-NMR and single crystal X-ray diffraction analysis. All the synthesized compounds were in vitro screened for antimicrobial activity against Gram-positive (Sarcina lutea) and Gram-negative bacteria (Escherichia coli). In this work, we introduced a chiral residue on the tetrahydropyridine nitrogen, the hitherto the less investigated position on this pharmacophore in order to explore the effect. The antibacterial results showed that the synthesized compounds were active only against Gram-positive bacteria and the (R)-enantiomers displayed a greater antimicrobial potency than their (S)-counterparts. The structure–activity relationship here investigated may provide some interesting clues for future development of tetrahydrothienopyridine derivatives with higher antimicrobial activity.

CONJUGATES OF KINASE INHIBITORS AND CYANINE DYES

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Paragraph 0406, (2019/11/22)

The present disclosure provides conjugates of kinase inhibitors and cyanine dyes, as well as related compositions, methods and uses.

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