158579-89-6 Usage
Uses
Used in Pharmaceutical Industry:
4-Chloro-2-(MethylsulfonaMido)benzoic Acid is used as a nonsteroidal anti-inflammatory drug (NSAID) for its ability to reduce pain, inflammation, and fever. It is particularly effective in treating conditions such as osteoarthritis, rheumatoid arthritis, and menstrual pain due to its inhibitory action on COX-1 and COX-2 enzymes involved in prostaglandin production.
Used in Pain Management:
4-Chloro-2-(MethylsulfonaMido)benzoic Acid is used as an analgesic agent to alleviate pain associated with various conditions, including musculoskeletal disorders and inflammatory diseases. Its dual inhibition of COX-1 and COX-2 enzymes contributes to its effectiveness in pain management.
Used in Inflammation Control:
4-Chloro-2-(MethylsulfonaMido)benzoic Acid is used as an anti-inflammatory agent to control inflammation in various conditions, such as arthritis and other inflammatory disorders. Its ability to inhibit prostaglandin production through the inhibition of COX enzymes helps in reducing inflammation and associated symptoms.
Used in Fever Reduction:
4-Chloro-2-(MethylsulfonaMido)benzoic Acid is used as an antipyretic agent to reduce fever by inhibiting the production of prostaglandins, which are responsible for the increase in body temperature during fever.
Check Digit Verification of cas no
The CAS Registry Mumber 158579-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,5,7 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 158579-89:
(8*1)+(7*5)+(6*8)+(5*5)+(4*7)+(3*9)+(2*8)+(1*9)=196
196 % 10 = 6
So 158579-89-6 is a valid CAS Registry Number.
158579-89-6Relevant academic research and scientific papers
4-benzoyl isoxazoles derivatives and their use as herbicides
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, (2008/06/13)
4-Benzoylisoxazole derivatives of the formula wherein R is H or an ester; R1is alkyl, haloalkyl or optionally substituted cycloalkyl; R2is halogen, optionally halogenated alkyl, alkenyl or alkynyl; alkyl substituted with one or more —OR5; —NO2, —CN, —CO2R5, —S(O)pR6, —O(CH2)mOR5, —COR5, —NR5R6, —N(R8)SOqR7, —CONR9R10or —OR51; or optionally substituted phenyl; R3is —S(O)qR7; X is —N(R8)—; n is 0, 1, 2, 3, or 4; R5, R51and R6are independently H; optionally halogenated alkyl, alkenyl or alkynyl; optionally substituted phenyl; or cycloalkyl; R7is optionally halogenated alkyl, alkenyl or alkynyl; cycloalkyl; optionally substituted phenyl; or optionally substituted amino; R8is H; optionally halogenated alkyl, alkenyl or alkynyl; cycloalkyl; optionally substituted phenyl; or alkoxy; m is 1, 2 or 3; p is 0, 1 or 2; q is 0 or 2; and their use as herbicides are described.
