103790-38-1 Usage
Description
METHYL 3-(4-AMINOPHENOXY)-2-THIOPHENECARBOXYLATE is a chemical compound characterized by the molecular formula C13H13NO3S. It is an ester formed by the combination of a methyl group, a carboxylic acid group, a thiophene ring, and an amino-phenoxy group. METHYL 3-(4-AMINOPHENOXY)-2-THIOPHENECARBOXYLATE is known for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as its utility in organic synthesis for creating biologically active compounds. Furthermore, it holds potential in materials science and as a reagent in chemical research.
Uses
Used in Pharmaceutical Synthesis:
METHYL 3-(4-AMINOPHENOXY)-2-THIOPHENECARBOXYLATE is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows it to be a key component in the development of new medications with specific therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, METHYL 3-(4-AMINOPHENOXY)-2-THIOPHENECARBOXYLATE serves as an intermediate in the production of pesticides and other agricultural chemicals. Its incorporation contributes to the effectiveness of these products in managing pests and diseases in crops.
Used in Organic Synthesis:
METHYL 3-(4-AMINOPHENOXY)-2-THIOPHENECARBOXYLATE is utilized as a building block in organic synthesis for the creation of a range of biologically active compounds. Its versatile chemical structure makes it a valuable component in the synthesis of molecules with potential applications in medicine and other fields.
Used in Materials Science:
METHYL 3-(4-AMINOPHENOXY)-2-THIOPHENECARBOXYLATE has potential applications in the field of materials science, where it may contribute to the development of new materials with unique properties. Its presence in these materials could enhance performance characteristics such as stability, reactivity, or selectivity.
Used as a Reagent in Chemical Research:
In chemical research, METHYL 3-(4-AMINOPHENOXY)-2-THIOPHENECARBOXYLATE is employed as a reagent to facilitate various chemical reactions and processes. Its reactivity and functional groups make it a useful tool for researchers in exploring new chemical pathways and syntheses.
Check Digit Verification of cas no
The CAS Registry Mumber 103790-38-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,9 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103790-38:
(8*1)+(7*0)+(6*3)+(5*7)+(4*9)+(3*0)+(2*3)+(1*8)=111
111 % 10 = 1
So 103790-38-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO3S/c1-15-12(14)11-10(6-7-17-11)16-9-4-2-8(13)3-5-9/h2-7H,13H2,1H3
103790-38-1Relevant articles and documents
Spirodienones. Part 5. The Synthesis and Reactions of N-Sulphonylcyclohexadienimines
Coutts, Ian G. C.,Culbert, Nicholas J.,Edwards, Mark,Hadfield, John A.,Musto, Donald R.,et al.
, p. 1829 - 1836 (2007/10/02)
The anodic or chemical oxidation of para-substituted sulphonanilides gives 4,4-disubstituted N-sulphonylcyclohexadienimines, which, from appropriately substituted anilines, may be spirocyclic.The scope and limitations of the synthesis are described, and mechanism proposed.The selective hydrolysis of the dienimines to the corresponding dienones provides a convenient route to the latter compounds.The reaction of some of the dienimines with dienes is discussed.
