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Pyridinium, 1-[2-(hydroxyimino)-2-phenylethyl]-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14181-82-9

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14181-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14181-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,8 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14181-82:
(7*1)+(6*4)+(5*1)+(4*8)+(3*1)+(2*8)+(1*2)=89
89 % 10 = 9
So 14181-82-9 is a valid CAS Registry Number.

14181-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-phenyl-2-pyridin-1-ium-1-ylethylidene)hydroxylamine,bromide

1.2 Other means of identification

Product number -
Other names -

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:14181-82-9 SDS

14181-82-9Relevant academic research and scientific papers

Synthesis, Isomerism, and Chemical Transformations of N-(2-Aryl-2-hydroxyiminoethyl) Azinium Salts

Artemov, V. A.,Shestopalov, A. M.,Litvinov, V. P.

, p. 548 - 553 (2007/10/03)

Quaternization of azines with ω-bromoacetophenone oximes yields N-(2-aryl-2-hydroxyiminoethyl)azinium salts, which exist as a mixtures of syn and anti isomers fixed due to interaction with the heteroring.The isomer ratio depends on the quaternization conditions and the substituent in the azine.N-(2-Aryl-2-hydroxyiminoethyl)azinium salts are deprotonated by bases, resulting in 1,4-elimination of the azine or ring closure into imidazoazines.

ON THE MECHANISM OF THE DECARBOXYLATIVE REARRANGEMENT OF THIOHYDROXAMIC ESTERS

Barton, Derek H.R.,Crich, David,Potier, Pierre

, p. 5943 - 5946 (2007/10/02)

The thermal and photochemical decomposition of a typical thiohydroxamic ester (mixed anhydride) doubly labelled with deuterium has shown the photochemical reaction to be a radical chain process, whereas about 20percent of the thermal reaction involves a cage mechanism.An improved route to 1-hydroxy-5-phenylthiazolin-2-thione is reported.

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