Welcome to LookChem.com Sign In|Join Free
  • or
4(7)-NITRO-2-METHYLBENZIMIDAZOLE is a chemical compound with the molecular formula C8H6N4O2, belonging to the benzimidazole family. It features a nitro group at the 4th or 7th position and a methyl group at the 2nd position, making it a versatile derivative with potential applications in various fields.

76320-88-2

Post Buying Request

76320-88-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

76320-88-2 Usage

Uses

Used in Pharmaceutical Industry:
4(7)-NITRO-2-METHYLBENZIMIDAZOLE is used as a building block for the synthesis of various drugs and bioactive molecules, contributing to the development of new pharmaceuticals.
Used in Organic Synthesis:
4(7)-NITRO-2-METHYLBENZIMIDAZOLE is used as a reagent in organic synthesis, facilitating the creation of a range of organic compounds.
Used in Dyes and Pigments Production:
4(7)-NITRO-2-METHYLBENZIMIDAZOLE is used as a starting material in the production of dyes and pigments, offering a foundation for the development of colorants for various applications.
Used in Medical Research and Drug Development:
Due to its pharmacological properties, 4(7)-NITRO-2-METHYLBENZIMIDAZOLE has potential applications in medical research and drug development, where it may contribute to the discovery and creation of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 76320-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,2 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76320-88:
(7*7)+(6*6)+(5*3)+(4*2)+(3*0)+(2*8)+(1*8)=132
132 % 10 = 2
So 76320-88-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O2/c1-5-9-6-3-2-4-7(11(12)13)8(6)10-5/h2-4H,1H3,(H,9,10)

76320-88-2Relevant academic research and scientific papers

REACTION OF ALIPHATIC AMINES WITH 2,3-DINITROACETANILIDE

Piotrovskii, L. B.

, p. 1458 - 1463 (2007/10/02)

In 2,3-dinitroacetanilide, ammonia and primary aliphatic amines substitute the nitro group at position 2, and secondary amines substitute the nitro group at position 3.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 76320-88-2