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122183-32-8

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122183-32-8 Usage

Structure

Quaternary ammonium salt with a pyridinium structure and a dimethylcarbamoyl group attached to the oxygen atom

Uses

a. Reagent in organic synthesis
b. Intermediate in the production of pharmaceuticals and agricultural chemicals

Properties

a. Antimicrobial
b. Antifungal

Industrial applications

Used as a biocide

Physical appearance

White crystalline solid

Solubility

Soluble in water and organic solvents

Check Digit Verification of cas no

The CAS Registry Mumber 122183-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,1,8 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122183-32:
(8*1)+(7*2)+(6*2)+(5*1)+(4*8)+(3*3)+(2*3)+(1*2)=88
88 % 10 = 8
So 122183-32-8 is a valid CAS Registry Number.

122183-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxypyridin-1-ium-1-yl) N,N-dimethylcarbamate,chloride

1.2 Other means of identification

Product number -
Other names Pyridinium,1-[[(dimethylamino)carbonyl]oxy]-4-methoxy-,chloride (1:1)

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:122183-32-8 SDS

122183-32-8Relevant articles and documents

INVESTIGATION OF THE STRUCTURE AND STATE OF N-CARBAMOYLONIUM SALTS IN NONAQUEOUS MEDIA BY 1H NMR SPECTROSCOPY

Lapshin, S. A.,Kapkan, L. M.,Fedorov, V. V.,Smirnov, Yu. I.

, p. 1857 - 1860 (2007/10/02)

The state of 1-carbamoyloxy-4-methoxypyridinium salts in CD3CN was studied by 1H NMR spectroscopy.It was shown that the most sensitive to concentration changes are the chemical shifts of the α- and β-protons and also the protons in the OCH3 group.The 1H NMR spectroscopic and thermodynamic parameters of the ionic dissociation of the salts were determined from the concentration dependence of the chemical shifts of the α-, β-, and OCH3-protons.

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