130525-39-2 Usage
Description
2,7-Di-tert-butyl-9,9-dimethyl-4,5-xanthenedicarboxylic acid is a carboxylic acid building block with a complex molecular structure featuring a xanthene core, tert-butyl groups, and dimethyl groups. 2,7-DI-TERT-BUTYL-9,9-DIMETHYL-4,5-XANTHENEDICARBOXYLIC ACID is characterized by its potential use in the synthesis of various organic compounds and materials.
Uses
Used in Chemical Synthesis:
2,7-Di-tert-butyl-9,9-dimethyl-4,5-xanthenedicarboxylic acid is used as a building block for the synthesis of complex organic molecules and materials. Its unique structure allows for the creation of a wide range of compounds with diverse properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,7-di-tert-butyl-9,9-dimethyl-4,5-xanthenedicarboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its structural versatility enables the development of new drugs with improved efficacy and reduced side effects.
Used in Material Science:
2,7-Di-tert-butyl-9,9-dimethyl-4,5-xanthenedicarboxylic acid is also utilized in the field of material science for the development of advanced materials with specific properties. These materials can be used in various applications, such as coatings, adhesives, and polymers, where their unique characteristics can provide enhanced performance.
Used in Dye Synthesis:
2,7-DI-TERT-BUTYL-9,9-DIMETHYL-4,5-XANTHENEDICARBOXYLIC ACID is used as a starting material in the synthesis of dyes, particularly those with specific color properties and stability. The dyes derived from 2,7-di-tert-butyl-9,9-dimethyl-4,5-xanthenedicarboxylic acid can be used in various industries, including textiles, plastics, and printing.
Used in Research and Development:
2,7-Di-tert-butyl-9,9-dimethyl-4,5-xanthenedicarboxylic acid is an important compound in research and development, where it is used to study the properties and behavior of complex organic molecules. This knowledge can lead to the discovery of new compounds and materials with novel applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 130525-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,2 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130525-39:
(8*1)+(7*3)+(6*0)+(5*5)+(4*2)+(3*5)+(2*3)+(1*9)=92
92 % 10 = 2
So 130525-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C25H30O5/c1-23(2,3)13-9-15(21(26)27)19-17(11-13)25(7,8)18-12-14(24(4,5)6)10-16(22(28)29)20(18)30-19/h9-12H,1-8H3,(H,26,27)(H,28,29)
130525-39-2Relevant articles and documents
Photocontrolled On-Surface Pseudorotaxane Formation with Well-Ordered Macrocycle Multilayers
Schwarz, Felix B.,Heinrich, Thomas,Kaufmann, J. Ole,Lippitz, Andreas,Puttreddy, Rakesh,Rissanen, Kari,Unger, Wolfgang E. S.,Schalley, Christoph A.
supporting information, p. 14383 - 14389 (2016/09/23)
The photoinduced pseudorotaxane formation between a photoresponsive axle and a tetralactam macrocycle was investigated in solution and on glass surfaces with immobilized multilayers of macrocycles. In the course of this reaction, a novel photoswitchable b
Convergent functional groups. 9. Complexation in new molecular clefts
Nowick, James S.,Ballester, Pablo,Ebmeyer, Frank,Rebek Jr., Julius
, p. 8902 - 8906 (2007/10/02)
Two new 2,7-di-tert-alkyl-9,9-dimethylxanthene-4,5-dicarboxylic acids are prepared as organic soluble, U-shaped modules for the construction of molecular hosts. Condensation of two diacid units with spacers (e.g., hydroquinone, 4,4′-biphenol, and 2,6-diaminonaphthalene) gives large structures capable of assuming cleftlike shapes that complex sizable guests such as DABCO, quinine, quinidine, and quinoxaline-2,3-dione. The xanthene diacids and their derivatives are shown to contain intramolecular hydrogen bonds that organize the binding sites and modify their chemical properties.
