213971-47-2 Usage
Uses
Used in Pharmaceutical Industry:
2,3-DiMethoxy-6-Methyl-7-(phenylMethyl)-4-propyl-1-naphthalenecarboxylic Acid is used as a key intermediate in the synthesis of lactate dehydrogenase A inhibitors for the pharmaceutical industry. Its role in the development of these inhibitors is essential for advancing research and potential treatments related to lactate dehydrogenase (LDH) enzymes.
Used in LDH-Related Research:
In the field of biochemical and medical research, 2,3-DiMethoxy-6-Methyl-7-(phenylMethyl)-4-propyl-1-naphthalenecarboxylic Acid is utilized as a vital component in the synthesis of compounds that target lactate dehydrogenase A. This contributes to a better understanding of LDH's role in various biological processes and the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 213971-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,9,7 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 213971-47:
(8*2)+(7*1)+(6*3)+(5*9)+(4*7)+(3*1)+(2*4)+(1*7)=132
132 % 10 = 2
So 213971-47-2 is a valid CAS Registry Number.
213971-47-2Relevant academic research and scientific papers
Hydroxynaphthoic acids and derivatives
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, (2008/06/13)
In one embodiment, the present invention provides a compound comprising: wherein A=H or OH X=OH, a halogen, OR, NHR, NR'R'' where R, R', and R''=H, C1-8 alkyl, C2-8 alkenyl, or C2-8 alkynyl, cycloalkyl, cycloalkenyl, aryl, aralkyl or heterocyclic, substit
Selective inhibitors of human lactate dehydrogenases and lactate dehydrogenase from the malarial parasite Plasmodium falciparum
Deck, Lorraine M.,Royer, Robert E.,Chamblee, Brian B.,Hernandez, Valerie M.,Malone, Richard R.,Torres, Jose E.,Hunsaker, Lucy A.,Piper, Robert C.,Makler, Michael T.,Vander Jagt, David L.
, p. 3879 - 3887 (2007/10/03)
Derivatives of the sesquiterpene 8-deoxyhemigossylic acid (2,3- dihydroxy-6-methyl-4-(1-methylethyl)-1-naphthoic acid) were synthesized that contained altered alkyl groups in the 4-position and contained alkyl or aralkyl groups in the 7-position. These su
