859212-59-2 Usage
Uses
Used in Pharmaceutical Chemistry:
ETHYL 3-IODO-4-METHYLBENZOATE is utilized as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new medications and therapeutic agents. Its unique structure allows for its incorporation into various drug molecules, enhancing their efficacy and pharmacological properties.
Used in Agrochemical Development:
In the agrochemical industry, ETHYL 3-IODO-4-METHYLBENZOATE serves as an essential component in the formulation of pesticides, herbicides, and other crop protection agents. Its integration into these products aids in improving their effectiveness in protecting crops from pests and diseases.
Used in Organic Synthesis:
ETHYL 3-IODO-4-METHYLBENZOATE is employed as a reagent in organic synthesis, facilitating various chemical reactions and transformations. Its presence can influence the outcome of these reactions, enabling the synthesis of complex organic molecules with specific functionalities.
Used in Material Science:
ETHYL 3-IODO-4-METHYLBENZOATE is used as a building block in the development of new materials with tailored properties. Its incorporation into these materials can lead to advancements in areas such as polymer science, nanotechnology, and the creation of substances with unique characteristics for specialized applications.
Used in Research and Development:
In the field of research and development, ETHYL 3-IODO-4-METHYLBENZOATE is leveraged as a valuable compound for exploring new chemical reactions, mechanisms, and the synthesis of novel organic compounds. Its use in this context aids scientists in expanding the frontiers of chemical knowledge and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 859212-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,9,2,1 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 859212-59:
(8*8)+(7*5)+(6*9)+(5*2)+(4*1)+(3*2)+(2*5)+(1*9)=192
192 % 10 = 2
So 859212-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11IO2/c1-3-13-10(12)8-5-4-7(2)9(11)6-8/h4-6H,3H2,1-2H3
859212-59-2Relevant academic research and scientific papers
Solid-phase synthesis of m-phenylene ethynylene heterosequence oligomers
Elliott, Erin L.,Ray, Christian R.,Kraft, Stefan,Atkins, Joseph R.,Moore, Jeffrey S.
, p. 5282 - 5290 (2007/10/03)
Both homo- and heterosequence m-phenylene ethynylene oligomers are synthesized using a conceptually simple iterative solid-phase strategy. Oligomers are attached to Merrifield's resin through a known triazene-type linkage. The phenylene ethynylene molecul
Design and synthesis of 3-substituted benzamide derivatives as Bcr-Abl kinase inhibitors
Asaki, Tetsuo,Sugiyama, Yukiteru,Hamamoto, Taisuke,Higashioka, Masaya,Umehara, Masato,Naito, Haruna,Niwa, Tomoko
, p. 1421 - 1425 (2007/10/03)
A series of 3-substituted benzamide derivatives structurally related to STI-571 (imatinib mesylate), a Bcr-Abl tyrosine kinase inhibitor used to treat chronic myeloid leukemia (CML), was prepared and evaluated for antiproliferative activity against the Bc
AMIDE DERIVATIVE AND MEDICINE
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Page/Page column 21, (2010/11/23)
The present invention is directed to an amide derivative having excellent BCR-ABL tyrosine kinase inhibitory activity, or a salt thereof. The present invention provides an amide derivative represented by the following general formula [1]: (wherein R1 represents -CH2-R11, etc.; R2 represents alkyl, halogen, haloalkyl, etc.; R3 represents hydrogen, etc.; Het1 represents a group of the formula [6] as above, etc.; and Het2 represents pyrimidinyl, etc.), or a pharmaceutically acceptable salt thereof, and a pharmaceutical composition comprising the same as an active ingredient. The compound of the present invention is useful as a BCR-ABL tyrosine kinase inhibitor.
