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6952-20-1

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6952-20-1 Usage

General Description

1,1,4,4-tetramethylpiperazindiium diiodide is an organic compound with the chemical formula (C8H20N2)I2. It is a derivative of piperazine, a heterocyclic compound commonly used in pharmaceuticals and organic synthesis. This particular compound is a diiodide salt, meaning it consists of two iodide ions for every molecule of the tetramethylpiperazindiium cation. It is commonly used as a catalyst in organic synthesis reactions, particularly as a source of diiodine, which is a powerful oxidizing agent. Additionally, it has potential applications in materials science and electrochemistry due to its unique redox properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6952-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6952-20:
(6*6)+(5*9)+(4*5)+(3*2)+(2*2)+(1*0)=111
111 % 10 = 1
So 6952-20-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H20N2/c1-9(2)5-7-10(3,4)8-6-9/h5-8H2,1-4H3/q+2

6952-20-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,4,4-tetramethylpiperazine-1,4-diium,diiodide

1.2 Other means of identification

Product number -
Other names 1,1,4,4-Tetramethylpiperazindiium diiodide

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:6952-20-1 SDS

6952-20-1Relevant articles and documents

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Smith et al.

, p. 2969 (1950)

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Spirocyclic meisenheimer complexes: XLII. Intramolecular alkylation of O-picryl amino alcohols with a tertiary amino group

Knyazev,Borbulevich,Shishkin

, p. 706 - 711 (2007/10/03)

Dimethyl(2-picryloxyethyl)-and dimethyl(3-picryloxypropyl)amines do not form zwitterionic spirocyclic 2,4,6-trinitrocyclohexadienide (Meisenheimer) adducts but undergo intramolecular alkylation to give, respectively, tetramethylpiperazinium and dimethylazetidinium picrates. Likewise, spirocyclic trinitrocyclohexadienide complex with a 4-morpholiniomethyl-1,3-dioxolane ring is regioselectively converted into 2-hydroxy-7-oxa-4-azoniaspiro[3.5]nonane picrate whose structure was proved by X-ray analysis.

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