844647-17-2 Usage
Description
2-Amino-4,5-dichloro-benzoic acid methyl ester is a chemical compound with the molecular formula C9H8Cl2NO2. It is a methyl ester derivative of 2-amino-4,5-dichlorobenzoic acid, characterized by its white to slightly off-white solid appearance and a melting point of around 200-202°C. This potentially hazardous substance requires careful handling to avoid skin, eye, and respiratory tract irritation.
Uses
Used in Pharmaceutical Research:
2-Amino-4,5-dichloro-benzoic acid methyl ester is utilized as a building block in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
In addition to pharmaceutical research, 2-amino-4,5-dichloro-benzoic acid methyl ester is also employed in the synthesis of agrochemical compounds. This enables the creation of new products for agricultural use, such as pesticides and herbicides, to improve crop protection and yield.
Used in Organic Synthesis:
2-Amino-4,5-dichloro-benzoic acid methyl ester serves as an important intermediate in organic synthesis, allowing for the production of a wide range of chemical compounds with various applications across different industries.
Used in Research Laboratories:
This chemical compound is commonly found in research laboratories, where scientists conduct experiments and studies to explore its potential applications and properties further.
Used in Chemical Manufacturing Facilities:
2-Amino-4,5-dichloro-benzoic acid methyl ester is also utilized in chemical manufacturing facilities for the large-scale production of pharmaceutical and agrochemical compounds, contributing to the development and supply of these essential products.
Check Digit Verification of cas no
The CAS Registry Mumber 844647-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,6,4 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 844647-17:
(8*8)+(7*4)+(6*4)+(5*6)+(4*4)+(3*7)+(2*1)+(1*7)=192
192 % 10 = 2
So 844647-17-2 is a valid CAS Registry Number.
844647-17-2Relevant articles and documents
NOVEL HISTONE METHYLTRANSFERASE INHIBITORS
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Page/Page column 30; 84, (2021/04/01)
The present invention relates to novel compounds of formula (I) as defined herein. The compounds are inhibitors of histone methyltransferases of the seven-beta-strand family, in particular of KMT9.
Hofmann-type rearrangement of imides by in situ generation of imide-hypervalent iodines(III) from iodoarenes
Moriyama, Katsuhiko,Ishida, Kazuma,Togo, Hideo
supporting information; experimental part, p. 946 - 949 (2012/05/05)
The Hofmann-type rearrangement of aromatic and aliphatic imides using a hypervalent iodine(III) reagent generated in situ from PhI, m-CPBA, and TsOH·H2O proceeded in the presence of a base in alcohol to provide anthranilic acid derivatives and amino acid derivatives in high yields, respectively. This reaction proceeds through a tandem reaction via alcoholysis followed by a Hofmann rearrangement promoted by the formation of an imide-λ3-iodane intermediate.
Anthranilic sulfonamide CCK1/CCK2 dual receptor antagonists II: Tuning of receptor selectivity and in vivo efficacy
Pippel, Marna,Boyce, Kristen,Venkatesan, Hariharan,Phuong, Victor K.,Yan, Wen,Barrett, Terrance D.,Lagaud, Guy,Li, Lina,Morton, Magda F.,Prendergast, Clodagh,Wu, Xiaodong,Shankley, Nigel P.,Rabinowitz, Michael H.
scheme or table, p. 6376 - 6378 (2010/05/02)
In the previous article we demonstrated how certain CCK2R-selective anthranilic amides could be structurally modified to afford high-affinity, selective CCK1R activity. We now describe our efforts at modulating and optimizing the CCK1R and CCK2R affinitie
