4389-53-1 Usage
Uses
Since the provided materials do not specify the uses of 2-Hydroxy-6-isopropyl-3-methylbenzoic acid, I will list potential applications based on its chemical structure and typical uses of similar compounds:
Used in Pharmaceutical Industry:
2-Hydroxy-6-isopropyl-3-methylbenzoic acid could be used as an intermediate in the synthesis of pharmaceutical compounds due to its unique structure, potentially contributing to the development of new drugs.
Used in Chemical Synthesis:
In the chemical industry, 2-Hydroxy-6-isopropyl-3-methylbenzoic acid might serve as a building block for the creation of various organic compounds, including dyes, fragrances, and additives.
Used in Material Science:
2-HYDROXY-6-ISOPROPYL-3-METHYLBENZOIC ACID could also be explored for its potential applications in material science, possibly for the development of new polymers or as a component in the formulation of specialty materials with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 4389-53-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4389-53:
(6*4)+(5*3)+(4*8)+(3*9)+(2*5)+(1*3)=111
111 % 10 = 1
So 4389-53-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O3/c1-6(2)8-5-4-7(3)10(12)9(8)11(13)14/h4-6,12H,1-3H3,(H,13,14)
4389-53-1Relevant academic research and scientific papers
Improved Preparation of the Clathrate Host Compound Tri-o-thymotide and Related Trisalicylide Derivatives
Gnaim, Jallal M.,Green, Bernard S.,Arad-Yellin, Rina,Keehn, Philip M.
, p. 4525 - 4529 (2007/10/02)
In order to improve the relatively low yield (ca. 35percent) previously observed in the synthesis of tri-o-thymotide (TOT, 1) from o-thymotic acid (2), the cyclodehydration was studied using a variety of conditions.The low yield is due to the formation of di-o-thymotide (DOT, 3), previously reported, and at least three other products (4-6), which apparently result from the acid-catalyzed decarboxylation of 2 and subsequent condensation with thymol (7).Using pyridine as a solvent, side-product formation is inhibited.Under appropriate conditions, namely, neat POCl3 at 50 deg C, the yield of 1 is 93percent.Other salicylic acid derivatives also give high yields of the corresponding "trimers" under these conditions, thus providing a general, improved preparation of a family of potential clathrate host substances.
