1886-79-9 Usage
Uses
Used in Pharmaceutical Industry:
3-(4-SULFAMOYL-PHENYLCARBAMOYL)-ACRYLIC ACID is used as a pharmaceutical compound for its potential inhibition properties against human carbonic anhydrase I and II isoenzymes. By targeting these enzymes, it may contribute to the development of new therapeutic strategies for conditions related to the dysregulation of these isoenzymes.
Used in Chemical Synthesis:
3-(4-SULFAMOYL-PHENYLCARBAMOYL)-ACRYLIC ACID can be utilized as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows for further functionalization and modification to create novel compounds with specific applications.
Used in Research and Development:
3-(4-SULFAMOYL-PHENYLCARBAMOYL)-ACRYLIC ACID serves as a valuable research tool for studying the structure-activity relationships of sulfonamide-based inhibitors and their interactions with target enzymes. It can also be used to develop new methodologies and techniques in organic synthesis and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1886-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1886-79:
(6*1)+(5*8)+(4*8)+(3*6)+(2*7)+(1*9)=119
119 % 10 = 9
So 1886-79-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O5S/c11-18(16,17)8-3-1-7(2-4-8)12-9(13)5-6-10(14)15/h1-6H,(H,12,13)(H,14,15)(H2,11,16,17)/b6-5-
1886-79-9Relevant articles and documents
The synthesis of (Z)-4-oxo-4-(arylamino)but-2-enoic acids derivatives and determination of their inhibition properties against human carbonic anhydrase I and II isoenzymes
Oktay, Koray,K?se, Leyla Polat,?endil, K?v?lc?m,Gültekin, Mehmet Serdar,Gül?in, ?lhami,Supuran, Claudiu T.
, p. 939 - 945 (2016/10/09)
The synthesis of (Z)-4-oxo-4-(arylamino)but-2-enoic acid (4) derivatives containing structural characteristics that can be used for the synthesis of several active molecules, is presented. Some of the butenoic acid derivatives (4a, 4c, 4e, 4i, 4j, 4k) are
Spectrophotometric and Titrimetric Determination of Carboxylic Acid Anhydrides
Verma, Krishna K.,Tyagi, Pramila
, p. 2157 - 2160 (2007/10/02)
Two redox methods are described for the determination of carboxylic acid anhydrides involving reaction with either an excess of 4-aminophenol or a measured but excessive amount of sulfanilamide and photometric titration of N-acyl-4-aminophenol with 2-iodylbenzoate by measuring the absorbance of orange-red product at 444 nm or the residual amount of sulfanilamide is determined by titration with chloramine-T in the presence of acidified potassium bromide using methyl red as visual indicator.Mixtures of certain anhydrides have also been analyzed by the 2-iodylbenzoate method.The methods are rapid, precise, and accurate.No correlation is needed if carboxylic and mineral acids are also present.Carboxylic acid chlorides also react quantitatively.
