3641-23-4 Usage
Uses
Used in Chemical Synthesis:
5-(Chloromethyl)-2-methoxybenzoic acid is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure, which includes a benzoic acid moiety and a chloromethyl group, makes it a valuable building block in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
5-(Chloromethyl)-2-methoxybenzoic acid is used as a key component in the development of new drugs. Its chemical properties, such as the ability to donate protons and its reactivity with other molecules, make it a promising candidate for the creation of novel therapeutic agents.
Used in Material Science:
5-(Chloromethyl)-2-methoxybenzoic acid is used as a functionalizing agent in the modification of materials. Its reactivity with other compounds allows for the introduction of new properties, such as improved thermal stability or enhanced chemical resistance, in materials used in various industries.
Used in Research and Development:
5-(Chloromethyl)-2-methoxybenzoic acid is used as a research compound in academic and industrial laboratories. Its unique structure and properties make it an interesting subject for studies in organic chemistry, materials science, and related fields.
While the practical applications and uses of 5-(Chloromethyl)-2-methoxybenzoic acid are not prominently documented, its chemical structure and properties suggest potential uses in various industries, including chemical synthesis, pharmaceutical development, material science, and research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 3641-23-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,4 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3641-23:
(6*3)+(5*6)+(4*4)+(3*1)+(2*2)+(1*3)=74
74 % 10 = 4
So 3641-23-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO3/c1-13-8-3-2-6(5-10)4-7(8)9(11)12/h2-4H,5H2,1H3,(H,11,12)
3641-23-4Relevant academic research and scientific papers
Design, synthesis and identification of novel colchicine-derived immunosuppressant
Chang, Dong-Jo,Yoon, Eun-Young,Lee, Geon-Bong,Kim, Soon-Ok,Kim, Wan-Joo,Kim, Young-Myeong,Jung, Jong-Wha,An, Hongchan,Suh, Young-Ger
scheme or table, p. 4416 - 4420 (2010/04/05)
Synthesis and biological evaluation of various colchicine analogues through the mixed-lymphocyte reaction (MLR), lymphoproliferation, and inhibitory effects on the inflammatory genes are described. In addition, a new series of immunosuppressive agents developed on the structural basis of colchicine, as well as their structure-activity relationships is reported. The most potent analogue 20a exhibited an excellent immunosuppressive activity on in vivo skin-allograft model, which is comparable to that of cyclosporin A.
