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1-(1-Methyl-5-nitro-1H-1,3-benzodiazol-2-yl)-ethan-1-ol is a chemical compound characterized by its benzodiazole core structure, featuring a nitro group and a methyl group, along with an ethan-1-ol side chain. 1-(1-Methyl-5-nitro-1H-1,3-benzodiazol-2-yl)-ethan-1-ol holds promise in the pharmaceutical industry due to the known biological activities and therapeutic properties of benzodiazole derivatives. The presence of the nitro group also suggests its potential use as a precursor in the synthesis of various pharmaceuticals, although further research and testing are required to explore its full potential.

2735-71-9

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2735-71-9 Usage

Uses

Used in Pharmaceutical Industry:
1-(1-Methyl-5-nitro-1H-1,3-benzodiazol-2-yl)-ethan-1-ol is used as a chemical compound for its potential biological activities and therapeutic properties. The benzodiazole core structure is known to contribute to the compound's effectiveness in various pharmaceutical applications.
Used as a Precursor in Synthesis:
In the pharmaceutical industry, 1-(1-Methyl-5-nitro-1H-1,3-benzodiazol-2-yl)-ethan-1-ol is used as a precursor for the synthesis of various pharmaceuticals, thanks to its nitro group, which can be further modified or utilized in the creation of new drug molecules.
Further Research and Testing:
1-(1-Methyl-5-nitro-1H-1,3-benzodiazol-2-yl)-ethan-1-ol is used in research and testing to fully understand its potential uses and effects, as the compound's properties and applications are not yet fully known and require additional investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 2735-71-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2735-71:
(6*2)+(5*7)+(4*3)+(3*5)+(2*7)+(1*1)=89
89 % 10 = 9
So 2735-71-9 is a valid CAS Registry Number.

2735-71-9Downstream Products

2735-71-9Relevant academic research and scientific papers

Syntheses of Substituted 2-(1-Methyl-5-nitro-2-benzimidazolyl)quinolines

Alimohammadi, F.,Abedifard, S.,Shafiee, A.

, p. 1037 - 1040 (2007/10/02)

Reaction of N-methyl-2-amino-4-nitroaniline (1) with lactic acid afforded 2-(1-hydroxyethyl)-1-methyl-5-nitrobenzimidazole (2).Oxidation of compound 2 with chromic acid in acetic acid gave 2-acetyl-1-methyl-5-nitrobenzimidazole (3).Reaction of compound 3

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