29043-48-9 Usage
Uses
Used in Pharmaceutical Industry:
1H-Benzimidazol-5-amine,2-methyl-(9CI) is utilized as a key intermediate in the synthesis of various pharmaceutical drugs. Its unique structure allows it to be incorporated into drug molecules, potentially enhancing their efficacy and selectivity for specific biological targets.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1H-Benzimidazol-5-amine,2-methyl-(9CI) serves as a building block for the design and development of new molecules with targeted biological activities. Its incorporation into drug candidates can lead to the discovery of novel therapeutic agents with improved pharmacological profiles.
Used in Drug Discovery:
1H-Benzimidazol-5-amine,2-methyl-(9CI) is employed in drug discovery processes to create new chemical entities with potential therapeutic applications. Its unique structural features make it a promising candidate for the development of innovative drugs that address unmet medical needs.
Organic Synthesis:
1H-Benzimidazol-5-amine,2-methyl-(9CI) is also used as a versatile building block in organic synthesis, enabling the creation of new molecules with specific biological activities. Its reactivity and structural attributes facilitate the synthesis of a wide range of compounds with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 29043-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,4 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29043-48:
(7*2)+(6*9)+(5*0)+(4*4)+(3*3)+(2*4)+(1*8)=109
109 % 10 = 9
So 29043-48-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3.ClH/c1-5-10-7-3-2-6(9)4-8(7)11-5;/h2-4H,9H2,1H3,(H,10,11);1H
29043-48-9Relevant academic research and scientific papers
THERMAL REACTIONS OF 1-ARYL-5-METHYLTETRAZOLES
Shurukhin, Yu. V.,Klyuev, N. A.,Grandberg, I. I.,Konchits, V. A.
, p. 1177 - 1182 (2007/10/02)
The mechanism of the thermal reactions of 1-aryl-5-methyltetrazoles, which involve isomerization to the azide, elimination of a nitrogen molecule, and formation of singlet nitrenes followed by isomerization to benzimidazoles and carbodiimides, has been studied by combinig the methods of derivatography and the current arsenal of mass-spectrometric techniques.The influence of the electronic properties of the substituent (in the para position of the benzene ring) on the course of the thermolysis has been established.
