1057652-84-2 Usage
General Description
Methyl 3-chloro-4-methyl-5-nitrobenzoate is a chemical compound with the molecular formula C9H8ClNO4. It is a derivative of benzoic acid and contains a methyl group, a chloro group, and a nitro group attached to a benzene ring. Methyl3-chloro-4-Methyl-5-nitrobenzoate is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various drugs and pharmaceuticals. It is also utilized as a chemical intermediate in the production of other organic compounds. Methyl 3-chloro-4-methyl-5-nitrobenzoate is considered a hazardous substance and should be handled with care and used in a controlled laboratory setting.
Check Digit Verification of cas no
The CAS Registry Mumber 1057652-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,7,6,5 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1057652-84:
(9*1)+(8*0)+(7*5)+(6*7)+(5*6)+(4*5)+(3*2)+(2*8)+(1*4)=162
162 % 10 = 2
So 1057652-84-2 is a valid CAS Registry Number.
1057652-84-2Relevant articles and documents
Aryl imidazole derivative and application thereof
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Paragraph 0567-00570, (2021/06/23)
The invention relates to an aryl imidazole derivative and application thereof. The aryl imidazole derivative is a compound shown as a formula (I) in the description or pharmaceutically acceptable salt thereof. The invention also discloses application of the aryl imidazole derivative in preparation of drugs for treating cancers. The invention further discloses application of the aryl imidazole derivative in preparation of drugs for treating diseases caused by EGFR mutation.
Orally active zwitterionic factor Xa inhibitors with long duration of action
Mochizuki, Akiyoshi,Nagata, Tsutomu,Kanno, Hideyuki,Takano, Daisuke,Kishida, Masamichi,Suzuki, Makoto,Ohta, Toshiharu
scheme or table, p. 7337 - 7343 (2012/02/04)
We have optimized 2-aminomethylphenylamine derivative as a factor Xa inhibitor. Several polar functional groups were introduced in the central phenyl ring, and we focused on zwitter ionic compound showing continuous inhibitory activity in oral administrat