34408-25-8 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
Methyl 2,5-dichloro-3-nitrobenzoate is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical properties make it a valuable component in the development of new drugs and agricultural products.
Used in Dye and Pigment Production:
methyl 2,5-dichloro-3-nitrobenzoate is employed as a key ingredient in the production of dyes and pigments. Its strong oxidizing properties contribute to the color intensity and stability of the final products.
Used in Organic Compound Manufacturing:
Methyl 2,5-dichloro-3-nitrobenzoate is also used in the manufacturing of other organic compounds. Its versatile chemical structure allows it to be incorporated into a wide range of organic synthesis processes, leading to the creation of various chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 34408-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,0 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34408-25:
(7*3)+(6*4)+(5*4)+(4*0)+(3*8)+(2*2)+(1*5)=98
98 % 10 = 8
So 34408-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Cl2NO4/c1-15-8(12)5-2-4(9)3-6(7(5)10)11(13)14/h2-3H,1H3
34408-25-8Relevant academic research and scientific papers
SUBSTITUTED BENZENE COMPOUNDS
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, (2012/11/06)
The present invention relates to substituted benzene compounds. The present invention also relates to pharmaceutical compositions containing these compounds and methods of treating cancer by administering these compounds and pharmaceutical compositions to subjects in need thereof. The present invention also relates to the use of such compounds for research or other non-therapeutic purposes.
ACYL GUANIDINE SODIUM/PROTON EXCHANGE INHIBITORS AND METHOD
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Page 42, (2010/02/10)
Acyl guanidines are provided which are sodium/proton exchange (NHE) inhibitors which have the structure wherein n is 1 to 5; X is N or C-R5 wherein R5 is H, halo, alkenyl, alkynyl, alkoxy, alkyl, aryl or heteroaryl; and R1, R2, R3 and R4 are as defined herein, and where X is N, R1 is preferably aryl or heteroaryl, and are useful as antianginal and cardioprotective agents. In addition, a method is provided for preventing or treating angina pectoris, cardiac dysfunction, myocardial necrosis, and arrhythmia employing the above acyl guanidines.
