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40188-34-9

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40188-34-9 Usage

General Description

2,4,6-trimethylbenzaldehyde oxime is a chemical compound with the formula C10H13NO. It is an oxime derivative of 2,4,6-trimethylbenzaldehyde and is used in organic synthesis as a building block for the preparation of various organic compounds. It is commonly used as a reagent in the preparation of N-heterocyclic carbene complexes, which are important intermediates in the synthesis of pharmaceuticals, agrochemicals, and materials. Additionally, 2,4,6-trimethylbenzaldehyde oxime has been studied for its potential use as a corrosion inhibitor in metal protection applications due to its ability to form protective films on metal surfaces. Overall, this compound has diverse applications in the field of organic chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 40188-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,8 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40188-34:
(7*4)+(6*0)+(5*1)+(4*8)+(3*8)+(2*3)+(1*4)=99
99 % 10 = 9
So 40188-34-9 is a valid CAS Registry Number.

40188-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-TRIMETHYL-BENZALDEHYDE OXIME

1.2 Other means of identification

Product number -
Other names (NE)-N-[(2,4,6-trimethylphenyl)methylidene]hydroxylamine

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:40188-34-9 SDS

40188-34-9Relevant articles and documents

Efficient transformation of electron-rich arenes into diethyl 3-arylisoxazole-4,5-dicarboxylates

Nakano, Ryuhta,Togo, Hideo

, (2020/05/26)

Treatment of electron-rich arenes with Tf2O and DMF, followed by the reaction with NH2OH·HCl and then with Oxone in the presence of diethyl acetylenedicarboxylate generated diethyl 3-arylisoxazole-4,5-dicarboxylates in good to modera

Initial steps in the reductive condensation of trichloromethylarenes with hydroxylamine and hydrazines in pyridine

Belen'kii, L. I.,Poddubnyi, I. S.,Krayushkin, M. M.

, p. 1844 - 1848 (2007/10/02)

Data concerning the initial steps in the reductive condensation of trichloromethylarenes with hydroxylamine or hydrazines in pyridine have been obtained.High yields of the products of the reductive condensation obtained even at equimolar ratios of trichloromethylarene with hydroxylamine or hydrazine as well as the formation of unusual products, i.e., 4-pyridylhydrazones of substituted benzaldehydes, have been interpreted as the results of the participation of pyridine in the reaction as a reductive agent. - Key words: trichloromethylarenes, reductive condensation with hydroxylamine or hydrazines, role of pyridine; 4-pyridylhydrazones of substituted benhaldehydes.

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