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4-Methoxy-3-Nitrobenzamide is an aromatic organic compound with the chemical formula C8H8N2O4. It features a methoxy group (OCH3), a nitro group (NO2), and an amide group (CONH2) attached to a benzene ring. 4-METHOXY-3-NITROBENZAMIDE is obtained through a nitration reaction of 4-methoxybenzoic acid, followed by an acylation. Due to its potential reactivity, proper safety measures should be taken when handling and using 4-Methoxy-3-Nitrobenzamide.

10397-58-7

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10397-58-7 Usage

Uses

Used in Organic Chemistry:
4-Methoxy-3-Nitrobenzamide is used as a synthetic intermediate for the synthesis of other complex molecules in the field of organic chemistry. Its unique functional groups allow for various chemical reactions and transformations, making it a valuable building block for the development of new compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-Methoxy-3-Nitrobenzamide is utilized as a starting material or intermediate in the synthesis of potential drug candidates. Its presence of different functional groups enables the design and development of molecules with specific biological activities, targeting various therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 10397-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10397-58:
(7*1)+(6*0)+(5*3)+(4*9)+(3*7)+(2*5)+(1*8)=97
97 % 10 = 7
So 10397-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O4/c1-14-7-3-2-5(8(9)11)4-6(7)10(12)13/h2-4H,1H3,(H2,9,11)

10397-58-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B24905)  4-Methoxy-3-nitrobenzamide, 97%   

  • 10397-58-7

  • 1g

  • 396.0CNY

  • Detail
  • Alfa Aesar

  • (B24905)  4-Methoxy-3-nitrobenzamide, 97%   

  • 10397-58-7

  • 5g

  • 1463.0CNY

  • Detail
  • Alfa Aesar

  • (B24905)  4-Methoxy-3-nitrobenzamide, 97%   

  • 10397-58-7

  • 25g

  • 6085.0CNY

  • Detail

10397-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-METHOXY-3-NITROBENZAMIDE

1.2 Other means of identification

Product number -
Other names 4-Methoxy-3-nitro-benzoesaeure-amid

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:10397-58-7 SDS

10397-58-7Relevant academic research and scientific papers

Iodine-catalyzed oxidative C-C bond cleavage for benzoic acids and benzamides from alkyl aryl ketones

Sathyanarayana, Pochampalli,Upare, Atul,Ravi, Owk,Muktapuram, Prathap Reddy,Bathula, Surendar Reddy

, p. 22749 - 22753 (2016/03/15)

Iodine-catalyzed oxidative C-C bond cleavage has been performed for the facile synthesis of both benzoic acids and benzamides from readily available alkyl aryl ketones. Additionally benzylidene acetones and phenylacetylenes were also converted to the corresponding aromatic acids under the same conditions. This approach features the use of inexpensive iodine as a catalyst, broad substrate scope and open air conditions.

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