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Methyl 2-amino-5-methyl-3-nitrobenzoate is a chemical compound with the molecular formula C9H10N2O4. It is a nitrobenzoate derivative characterized by a methyl group at the 2-position and an amino group at the 5-position of the benzene ring. methyl 2-amino-5-methyl-3-nitrobenzoate is recognized for its potential as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it is studied for its biological activity and potential therapeutic properties. However, due to its potential hazards, it is crucial to handle this chemical with care.

1248541-72-1

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1248541-72-1 Usage

Uses

Used in Organic Synthesis:
Methyl 2-amino-5-methyl-3-nitrobenzoate is used as a key intermediate in organic synthesis for the production of a variety of compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, methyl 2-amino-5-methyl-3-nitrobenzoate is utilized as a building block for the development of new drugs. Its presence in the molecular structure can contribute to the pharmacological properties of the final product, aiding in the discovery of novel therapeutic agents.
Used in Agrochemical Development:
Methyl 2-amino-5-methyl-3-nitrobenzoate is also employed in the agrochemical sector, where it serves as a precursor in the synthesis of various agrochemicals. Its application in this field is crucial for the development of new pesticides and other agricultural chemicals that can improve crop protection and yield.
Used in Fine Chemicals Production:
methyl 2-amino-5-methyl-3-nitrobenzoate is used as a raw material in the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, fragrances, and flavors. The versatility of methyl 2-amino-5-methyl-3-nitrobenzoate makes it suitable for the synthesis of a wide range of specialty chemicals.
Used in Biological Activity Studies:
Methyl 2-amino-5-methyl-3-nitrobenzoate is studied for its biological activity, which may lead to the discovery of new therapeutic properties. Research in this area can potentially uncover its applications in medicine and other biological fields, expanding its uses beyond traditional chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1248541-72-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,8,5,4 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1248541-72:
(9*1)+(8*2)+(7*4)+(6*8)+(5*5)+(4*4)+(3*1)+(2*7)+(1*2)=161
161 % 10 = 1
So 1248541-72-1 is a valid CAS Registry Number.

1248541-72-1Relevant academic research and scientific papers

BENZIMIDAZOLES DERIVATIVES AS ANTI-TUBERCULOSIS AGENTS

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, (2020/10/09)

The present invention provides novel compounds of benzimidazole derivatives as anti-tubercular agents and their pharmaceutically acceptable salts for use as bactericidal therapeutics. The invention also provides a pharmaceutical composition comprising a c

Scaffold Morphing To Identify Novel DprE1 Inhibitors with Antimycobacterial Activity

Manjunatha,Shandil, Radha,Panda, Manoranjan,Sadler, Claire,Ambady, Anisha,Panduga, Vijender,Kumar, Naveen,Mahadevaswamy, Jyothi,Sreenivasaiah,Narayan, Ashwini,Guptha, Supreeth,Sharma, Sreevalli,Sambandamurthy, Vasan K.,Ramachandran, Vasanthi,Mallya, Meenakshi,Cooper, Christopher,Mdluli, Khisi,Butler, Scott,Tommasi, Ruben,Iyer, Pravin S.,Narayanan, Shridhar,Chatterji, Monalisa,Shirude, Pravin S.

, p. 1480 - 1485 (2019/10/19)

We report a novel benzimidazole (BI) based DprE1 inhibitor that resulted from scaffold morphing of a 1,4-azaindole series. The clinical progression of the 1,4-azaindole series from our previous work validates the potential of exploring newer chemical enti

Design and synthesis of 2-(4,5,6,7-tetrahydrothienopyridin-2-yl)-benzoimidazole carboxamides as novel orally efficacious Poly(ADP-ribose)polymerase (PARP) inhibitors

Chen, Xuxing,Huan, Xiajuan,Liu, Qiufeng,Wang, Yuqin,He, Qian,Tan, Cun,Chen, Yi,Ding, Jian,Xu, Yechun,Miao, Zehong,Yang, Chunhao

, p. 389 - 403 (2018/01/17)

The nuclear protein poly(ADP-ribose) polymerases-1/2 (PARP-1/2) are involved in DNA repair damaged by endogenous or exogenous process. And PARP-1/2 inhibitors have been proved to be clinically efficacious for DNA repair deficient tumors in the past decade

DIHYDROOROTATE DEHYDROGENASE INHIBITORS

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Page/Page column 78-79, (2010/11/03)

The invention relates to compounds of formula (I) wherein R1, R2, X1, X2, Y, Ra, Rb, Q have the meanings given in claim 1. The compounds are useful e.g. in the treatment of autoimmune disorders, such as multiple sclerosis and also in the treatment of cancer disorders.

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