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92-20-6

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92-20-6 Usage

General Description

2',5'-dimethoxy-4'-nitrobenzanilide is a chemical compound with the molecular formula C15H14N2O5. It is a member of the anilide class of compounds and is commonly used in organic chemistry research. 2',5'-dimethoxy-4'-nitrobenzanilide is a yellow solid that is insoluble in water but soluble in organic solvents such as acetone and ethanol. It is known for its strong electron-withdrawing nitro group and its methoxy substituents, which give it particular reactivity in certain chemical reactions. 2',5'-dimethoxy-4'-nitrobenzanilide is often used as a reagent in synthetic organic chemistry and is useful for the synthesis and modification of other organic compounds.

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92-20-6 SDS

92-20-6Relevant articles and documents

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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