1201597-23-0 Usage
Description
2,6-Difluoro-4-methylbenzoic acid is a chemical compound with the molecular formula C8H6F2O2. It is an aromatic carboxylic acid that features a benzoic acid core with a methyl group and two fluorine atoms at the 2nd and 6th positions. The presence of fluorine atoms contributes to its partial volatility. 2,6-Difluoro-4-methylbenzoic acid is primarily used in chemical syntheses and research, serving as an intermediate in organic chemistry.
Uses
Used in Chemical Synthesis:
2,6-Difluoro-4-methylbenzoic acid is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows for the creation of a range of derivatives, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research Contexts:
In the field of organic chemistry, 2,6-difluoro-4-methylbenzoic acid is used as a research compound to study the effects of fluorination on the properties of aromatic systems. Its reactivity and the influence of the fluorine atoms on the molecule's behavior are of particular interest to chemists.
Used in Pharmaceutical Development:
2,6-Difluoro-4-methylbenzoic acid is used as a building block in the development of new pharmaceuticals. Its structural characteristics can be exploited to design drugs with improved potency, selectivity, and bioavailability.
Used in Agrochemical Production:
2,6-Difluoro-4-methylbenzoic acid is also used in the agrochemical industry as a precursor for the synthesis of new pesticides and herbicides. The introduction of fluorine atoms can enhance the biological activity and environmental stability of these agrochemicals.
Note: The effects and potential hazards of 2,6-difluoro-4-methylbenzoic acid to human health or the environment have not been extensively studied. Therefore, strict handling and disposal procedures are often recommended as a precaution.
Check Digit Verification of cas no
The CAS Registry Mumber 1201597-23-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,5,9 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1201597-23:
(9*1)+(8*2)+(7*0)+(6*1)+(5*5)+(4*9)+(3*7)+(2*2)+(1*3)=120
120 % 10 = 0
So 1201597-23-0 is a valid CAS Registry Number.
1201597-23-0Relevant articles and documents
Asymmetric Total Synthesis of (-)-Maldoxin, a Common Biosynthetic Ancestor of the Chloropupukeananin Family
Suzuki, Takahiro,Watanabe, Soichiro,Uyanik, Muhammet,Ishihara, Kazuaki,Kobayashi, Susumu,Tanino, Keiji
supporting information, p. 3919 - 3922 (2018/07/25)
The total synthesis of pestheic acid based on an intramolecular SNAr reaction without a nitro group and the asymmetric synthesis of (-)-maldoxin by a catalytic enantioselective oxidative dearomatization of pestheic acid are described. The reactivity of (-)-maldoxin as a diene in the Diels-Alder reaction is also investigated.
PYRROLO [2, 3-C] PYRIDINE DERIVATIVES AS P38 KINASE INHIBITING AGENTS
-
Page/Page column 35, (2010/01/07)
Compounds described by the chemical formula (I) or pharmaceutically acceptable salts thereof: (A) are inhibitors of p38 and are useful in the treatment of inflammation such as in the treatment of asthma, rheumatoid arthritis, rheumatoid spondylitis, osteoarthritis, gouty arthritis and other arthritic conditions; inflamed joints, eczema, psoriasis or other inflammatory skin conditions such as sunburn; inflammatory eye conditions including conjunctivitis; pyresis, pain and other conditions associated with inflammation.
