473-35-8 Usage
Explanation
Different sources of media describe the Explanation of 473-35-8 differently. You can refer to the following data:
1. This is the scientific name of the chemical compound, also known as carprofen.
2. Carprofen belongs to a class of drugs called NSAIDs, which are used to reduce inflammation and pain.
3. Carprofen is primarily used to alleviate pain and inflammation in veterinary patients, specifically dogs and cats.
4. Carprofen works by inhibiting the production of prostaglandins, substances in the body that cause pain and inflammation.
5. Carprofen is often prescribed for the treatment of various conditions in animals, such as arthritis, pain after surgery, and other issues related to the muscles and skeleton.
6. The chemical structure of carprofen includes a carboxycyclopentyl group and a methylpropionic acid group, which are essential for its pharmacological activity and effectiveness.
7. It is important to use carprofen under the supervision of a veterinarian to avoid potential side effects and interactions with other medications.
Classification
Nonsteroidal anti-inflammatory drug (NSAID)
Usage
Relief of pain and inflammation in dogs and cats
Mechanism of action
Inhibition of prostaglandin production
Common uses
Treatment of arthritis, post-operative pain, and musculoskeletal conditions
Chemical structure
Carboxycyclopentyl group and methylpropionic acid group
Safety precautions
Use under the guidance of a veterinarian
Check Digit Verification of cas no
The CAS Registry Mumber 473-35-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 473-35:
(5*4)+(4*7)+(3*3)+(2*3)+(1*5)=68
68 % 10 = 8
So 473-35-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O4/c1-10(2,9(13)14)7-4-3-6(5-7)8(11)12/h6-7H,3-5H2,1-2H3,(H,11,12)(H,13,14)
473-35-8Relevant articles and documents
NATURAL PRODUCT SYNTHESIS VIA THE POLYBROMO KETONE-IRON CARBONYL REACTION
Noyori, R.,Hayakawa, Y.
, p. 5879 - 5886 (2007/10/02)
Application of the polybromo ketone-iron carbonyl reaction to natural product synthesis is summarized.The general synthesis of tropane alkaloids has been achieved via the reductive cyclocoupling of sym-tetrabromoacetone with N-methoxycarbonylpyrrole as the key step.Ready availability of 8-oxabicyclooct-6-en-3-one from the tetrabromoacetone and furan has opened a new, efficient entry to natural C-nucleosides including pseudouridine, pseudocytidine, and showdomycin.The artificial analogues such as 2-thiopseudouridine, 6-azapseudouridine, pseudoisocytidine, etc., are also obtainable.The oxabicyclic ketones bearing an isopropyl substituent at the appropriate position serve as intermediates for the synthesis of naturally occurring troponoids, nezukone, α-thujaplicin, and hinokitiol (β-thujaplicin).Carbocamphenilone and camphenic acid have been prepared through the reaction of 1,1,3-tribromo-3-methylbutan-2-one and cyclopentadiene.The cyclocondensation of α,α'-dibromo ketone and a styrene derivative leads to the single-step synthesis of α-cuparenone. 1,3-Dibromo-3,7-dimethyloct-6-en-2-one derived from nerol (or geraniol) undergoes the biogenetic-type double cyclization.The iron carbonyl-assisted intramolecular cyclocoupling gives camphor accompanied by other monoterpenic ketones.A mixture of campherenone and epicampherenone has been obtained from related dibromo ketone prepared from farnesols.The hetero reaction by use of dibromo ketones and N,N-dimethylcarboxamides, forming 3 (2H)-furanones, is employable for the preparation of muscarine alkaloid derivatives.
