1996-51-6 Usage
Description
4-AMINO-3-CHLOROBENZENESULFONYL FLUORIDE, also known as ACBFL, is a versatile chemical compound that serves as a crucial reagent in organic synthesis. It is characterized by its white solid form, solubility in organic solvents, and a low melting point. ACBFL is recognized for its role as an important intermediate in the synthesis of a variety of products, including pharmaceuticals, agrochemicals, and dyes. Its utility extends to the production of specialty and fine chemicals, where it introduces the sulfonyl fluoride functional group into organic molecules, establishing it as a significant building block in the creation of complex organic compounds. Furthermore, ACBFL is valued for its inhibitory properties against enzymes such as matrix metalloproteinases and serine proteases.
Uses
Used in Pharmaceutical Industry:
4-AMINO-3-CHLOROBENZENESULFONYL FLUORIDE is used as a synthetic intermediate for the development of various pharmaceuticals, leveraging its ability to introduce the sulfonyl fluoride group into organic molecules, which is essential for the creation of new drug candidates.
Used in Agrochemical Industry:
In the agrochemical sector, 4-AMINO-3-CHLOROBENZENESULFONYL FLUORIDE is utilized as a key component in the synthesis of agrochemicals, contributing to the development of effective pest control agents and other agricultural products.
Used in Dye Industry:
4-AMINO-3-CHLOROBENZENESULFONYL FLUORIDE is employed as a critical intermediate in the production of dyes, where its chemical properties are harnessed to create a spectrum of colorants for various applications.
Used in Specialty and Fine Chemicals Production:
ACBFL is used as a versatile building block in the synthesis of specialty and fine chemicals, where its introduction of the sulfonyl fluoride functional group is crucial for the development of high-value chemical products.
Used as an Enzyme Inhibitor:
4-AMINO-3-CHLOROBENZENESULFONYL FLUORIDE is used as an inhibitor for enzymes such as matrix metalloproteinases and serine proteases, playing a significant role in biological research and the development of therapeutic agents targeting these enzymes.
Check Digit Verification of cas no
The CAS Registry Mumber 1996-51-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1996-51:
(6*1)+(5*9)+(4*9)+(3*6)+(2*5)+(1*1)=116
116 % 10 = 6
So 1996-51-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H10F3NO4/c1-21-10-3-5-11(6-4-10)22-13-7-2-9(14(15,16)17)8-12(13)18(19)20/h2-8H,1H3
