349626-29-5 Usage
Description
2-[(N-acetyl-sulfanilyl)-amino]-thiazol-4-yl-acetic acid ethyl ester is a complex chemical compound characterized by a thiazole ring with an amino group and an acetyl-sulfanilyl group attached to it. It also features an acetic acid group and an ethyl ester group, which may contribute to its potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
2-[(N-acetyl-sulfanilyl)-amino]-thiazol-4-yl-acetic acid ethyl ester is used as a potential pharmaceutical compound for its possible therapeutic properties. 2-[(N-acetyl-sulfanilyl)-amino]-thiazol-4-yl-acetic acid ethyl ester's unique structure may allow it to interact with biological targets, potentially leading to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, 2-[(N-acetyl-sulfanilyl)-amino]-thiazol-4-yl-acetic acid ethyl ester may be used as a precursor for the synthesis of various agrochemical products, such as pesticides or herbicides. Its complex structure could provide novel modes of action or improved efficacy in these applications.
Used in Chemical Research:
2-[(N-acetyl-sulfanilyl)-amino]-thiazol-4-yl-acetic acid ethyl ester can be used as a research compound for studying its chemical properties and potential reactions with other molecules. This may lead to the discovery of new chemical processes or the development of new materials.
Note: The uses listed above are speculative based on the compound's structure and the general applications of similar compounds. Further research and testing are required to confirm the compound's properties and potential applications in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 349626-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,6,2 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 349626-29:
(8*3)+(7*4)+(6*9)+(5*6)+(4*2)+(3*6)+(2*2)+(1*9)=175
175 % 10 = 5
So 349626-29-5 is a valid CAS Registry Number.
349626-29-5Relevant articles and documents
Hapten synthesis and development of polyclonal antibody-based multi-sulfonamide immunoassays
Zhang, Hongyan,Duan, Zhenjuan,Wang, Lei,Zhang, Yan,Wang, Shuo
, p. 4499 - 4505 (2006)
This paper reports the synthesis of five sulfonamide derivatives, the production of broad-specificity polyclonal antibodies for immunoassay of sulfonamides, and the analysis of milk samples by developed assay. The three-step synthesis procedure reported in most of the literature was adopted and modified in this study. In the procedure, the purification of the intermediate was avoided and the time of synthesis was shortened from >20 to 6-9 h with improved yields. This method is generally applicable to the synthesis of haptens containing the common structure of sulfonamides. Three haptens were coupled to keyhole limpet hemocyanin, and polyclonal antibodies were obtained from rabbits immunized with these conjugates. Using the antibodies obtained, from one of these was developed an enzyme-linked immunosorbent assay (ELISA) based on the competition between free sulfonamides and the hapten-horseradish peroxidase (HRP) conjugates. The hapten-HRP conjugate giving the best competitive results and 11 structurally different sulfonamides showed 50% inhibition at concentrations of -1. After removal of the protein with acetone, milk samples were analyzed by ELISA directly; a matrix effect could be avoided when a 1:20 dilution with phosphate-buffered saline was used, and 104-131% recoveries of spiked samples were obtained. The developed immunoassay is suitable to determine sulfisozole, sulfathiazole, sulfameter, sulfamethoxypyridazine, sulfapyridine, and sulfamethizole below the maximum residue limit in milk (100 ng mL-1 of total sulfonamides) rapidly and reliably.
