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2',5'-dimethoxy-4'-nitrobenzanilide is a chemical compound belonging to the anilide class, characterized by its molecular formula C15H14N2O5. It is a yellow solid that is insoluble in water but soluble in organic solvents like acetone and ethanol. 2',5'-dimethoxy-4'-nitrobenzanilide is distinguished by its strong electron-withdrawing nitro group and methoxy substituents, which confer specific reactivity in various chemical reactions.

92-20-6

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92-20-6 Usage

Uses

Used in Organic Chemistry Research:
2',5'-dimethoxy-4'-nitrobenzanilide is utilized as a reagent in synthetic organic chemistry, playing a crucial role in the synthesis and modification of other organic compounds. Its unique properties make it a valuable component in the development of new chemical entities and the study of reaction mechanisms in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 92-20-6 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92-20:
(4*9)+(3*2)+(2*2)+(1*0)=46
46 % 10 = 6
So 92-20-6 is a valid CAS Registry Number.

92-20-6SDS

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 2',5'-Dimethoxy-4'-nitrobenzanilide

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

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More Details:92-20-6 SDS

92-20-6Relevant academic research and scientific papers

Reactions of some N-(2,5-dimethoxyaryl)thiobenzamides: En route to an analogue of kuanoniamine A

Jackson, Yvette A.,Lyon, Michael A.,Townsend, Norman,Bellabe, Kettyna,Soltanik, Fernando

, p. 205 - 210 (2007/10/03)

The reactions of some N-(2,5-dimethoxyaryl) thiobenzamides were studied. It was found that nitration of 2-aryl-4,7-dimethoxybenzothiazoles produced a mixture of 5- and 6-nitrobenzothiazoles which were distinguished by synthesis of the 2-aryl-4,7-dimethoxy-6-nitrobenzothiaoles by oxidative cyclization of the corresponding nitrothiobenzanilides. The results showed that the cyclization of arylthioanilides was influenced by the nature of the ring substituents.

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