4399-52-4 Usage
Uses
Used in Immune System Support:
TRI-O-THYMOTIDE is used as an immune system booster for its ability to increase the production of white blood cells, which are essential in fighting off infections and diseases. The synergistic action of the three thymus extracts in TRI-O-THYMOTIDE makes it an effective supplement for enhancing immune function and supporting overall health.
Used in Health and Wellness Industry:
In the health and wellness industry, TRI-O-THYMOTIDE is used as a comprehensive health supplement for its potential to improve energy levels, reduce inflammation, and support optimal cellular function. The unique blend of thymus extracts in TRI-O-THYMOTIDE contributes to overall well-being and promotes a healthy lifestyle.
Used in Anti-Inflammatory Applications:
TRI-O-THYMOTIDE is used as an anti-inflammatory agent due to its potential to reduce inflammation, which can contribute to various health issues if left uncontrolled. The thymus extracts in TRI-O-THYMOTIDE may help alleviate inflammation and support a healthy inflammatory response in the body.
Used in Cellular Function Support:
TRI-O-THYMOTIDE is used as a cellular function support agent for its potential to promote optimal cellular function. The unique blend of thymus extracts in TRI-O-THYMOTIDE may help maintain the normal functioning of cells, contributing to overall health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 4399-52-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,9 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4399-52:
(6*4)+(5*3)+(4*9)+(3*9)+(2*5)+(1*2)=114
114 % 10 = 4
So 4399-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C33H36O6/c1-16(2)22-13-10-19(7)25-28(22)37-32(35)26-20(8)11-14-23(17(3)4)29(26)39-33(36)27-21(9)12-15-24(18(5)6)30(27)38-31(25)34/h10-18H,1-9H3
4399-52-4Relevant academic research and scientific papers
Halogenated analogs of tri-O-thymotide (TOT) and Tri-3-(2-butyl)-6-methylsalicylide (TSBS): Synthesis and clathration studies
Gnaim,Keehn,Green
, p. 2883 - 2886 (2007/10/02)
Halogenated trisalicylide derivatives 1-6, representing three-fold symmetric C3 'homo trimers' as well as dissymmetric C1 'mixed trimers' have been synthesized. Clathration studies indicate that these halogenated TOT analogs do not f
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.
