39977-41-8 Usage
General Description
5-(hydroxyMethyl)picolinic acid is a chemical compound with the molecular formula C7H7NO3. It belongs to the class of picolinic acids and contains a hydroxymethyl group attached to the 5-position of the picolinic acid. 5-(hydroxyMethyl)picolinic acid has potential applications in the pharmaceutical industry, as it is known to have antioxidant and chelating properties. It may also be used in the synthesis of coordination complexes and metal-based drugs. Additionally, 5-(hydroxyMethyl)picolinic acid has been studied for its potential role in treating conditions related to metal ion imbalances in the body, making it a subject of interest for further research in the field of medicine and biochemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 39977-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,7 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39977-41:
(7*3)+(6*9)+(5*9)+(4*7)+(3*7)+(2*4)+(1*1)=178
178 % 10 = 8
So 39977-41-8 is a valid CAS Registry Number.
39977-41-8Relevant articles and documents
Sulfonamides
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Page/Page column 40, (2010/02/15)
The invention relates to compounds of the general formula in which R1, R2, R3, R4, R2′, R3′, R4′, R5, and X is —CHR— are as defined in the specification. The invention also provides pharmac
Aromatic Retinoic Acid Analogues. 2. Synthesis and Pharmacological Activity
Dawson, Marcia I.,Chan, Rebecca,Hobbs, Peter D.,Chao, Wan-ru,Schiff, Leonard J.
, p. 1282 - 1293 (2007/10/02)
Aromatic analogues of (E)-1-(4-carboxyphenyl)-2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)butadiene (1b) and its ethyl ester (1a) were synthesized as potential chemopreventive agents for the treatment of epithelial cancer and such skin diseases as psoriasis and cystic acne.The phenyl ring of 1 was replaced by 2-fluorophenyl, 2-methoxyphenyl, thienyl, furanyl, and pyridyl groups.The 1-fluorobutadiene analogue of 1 was also synthesized.With exception for the furanyl analogue, these compounds demonstrated good activity in reversing keratinization in hamster tracheal organ culture and in inhibiting the induction of ornithine decarboxylase in mouse epidermis by a tumor promoter.
