3641-23-4 Usage
General Description
5-(Chloromethyl)-2-methoxybenzoic acid, a slightly yellow powdery substance, belongs to the class of organic compounds known as benzoic acids. It is also classified as a halobenzoic acid. 5-(Chloromethyl)-2-methoxybenzoic acid includes a benzoic acid moiety, which is a compound containing a benzene ring attached to a carboxylic acid group, and a halogen atom (in this case, chlorine). Its methoxy functionality, which includes a methyl group attached to an oxygen atom, further adds to its chemical structure. Being an acid, this chemical compound can donate protons and can potentially function as a corrosive agent. Despite its name, the compound is not entirely made of chlorine, methyl, oxygen, and benzoic acid. It primarily consists of hydrogen and carbon. Being methoxylated means it contains an oxygen atom bonded to a methyl group. Its practical applications and uses, however, are not prominently documented.
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 articles and documents
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.
