100858-27-3 Usage
Description
t-Butyl-3-[2-(diphenyl-phosphinoyl)-ethylidene]-4-methylene-cyclohexyloxy-dimethyl-silane is a complex organic compound with a unique molecular structure. It is characterized by a tert-butyl group, a diphenyl-phosphinoyl-ethylidene group, a 4-methylene-cyclohexyloxy group, and a dimethyl-silane group. tert-Butyl-3-[2-(diphenyl-phosphinoyl)-ethylidene]-4-methylene-cyclohexyloxy-dimethyl-silane is known for its potential applications in various chemical and pharmaceutical processes due to its versatile functional groups and unique reactivity.
Uses
1. Used in Pharmaceutical Industry:
t-Butyl-3-[2-(diphenyl-phosphinoyl)-ethylidene]-4-methylene-cyclohexyloxy-dimethyl-silane is used as an intermediate in the synthesis of Vitamin D3 derivatives for its ability to contribute to the formation of complex molecular structures required in the pharmaceutical industry.
2. Used in Chemical Synthesis:
In the chemical synthesis industry, t-Butyl-3-[2-(diphenyl-phosphinoyl)-ethylidene]-4-methylene-cyclohexyloxy-dimethyl-silane is used as a versatile building block for creating a wide range of compounds. Its unique structure allows for various reactions, making it a valuable component in the synthesis of complex organic molecules.
3. Used in Catalyst Development:
The compound's phosphinoyl group makes it a potential candidate for use in the development of catalysts, particularly in transition metal-catalyzed reactions. Its ability to form stable complexes with metal centers can enhance the efficiency and selectivity of catalytic processes.
4. Used in Material Science:
Due to its silane group, t-Butyl-3-[2-(diphenyl-phosphinoyl)-ethylidene]-4-methylene-cyclohexyloxy-dimethyl-silane can be utilized in the development of new materials with specific properties, such as improved thermal stability or enhanced chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 100858-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,5 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100858-27:
(8*1)+(7*0)+(6*0)+(5*8)+(4*5)+(3*8)+(2*2)+(1*7)=103
103 % 10 = 3
So 100858-27-3 is a valid CAS Registry Number.
InChI:InChI=1/C27H37O2PSi/c1-22-17-18-24(29-31(5,6)27(2,3)4)21-23(22)19-20-30(28,25-13-9-7-10-14-25)26-15-11-8-12-16-26/h7-16,19,24H,1,17-18,20-21H2,2-6H3/b23-19-/t24-/m0/s1
100858-27-3Relevant articles and documents
Chemical synthesis, biological activities and action on nuclear receptors of 20S(OH)D3, 20S,25(OH)2D3, 20S,23S(OH)2D3 and 20S,23R(OH)2D3
Atigadda, Venkatram,Brzeminski, Pawel,Fabisiak, Adrian,Janjetovic, Zorica,Jetten, Anton M.,Kim, Tae-Kang,Podgorska, Ewa,Qayyum, Shariq,Raman, Chander,Reddy, Sivani B.,Saleem, Mohammad,Sicinski, Rafal R.,Slominski, Andrzej T.,Slominski, Radomir M.,Song, Yuhua,Song, Yuwei,Tuckey, Robert C.
supporting information, (2022/02/17)
New and more efficient routes of chemical synthesis of vitamin D3 (D3) hydroxy (OH) metabolites, including 20S(OH)D3, 20S,23S(OH)2D3 and 20S,25(OH)2D3, that are endogenously prod
Synthesis of Retiferol RAD1 and RAD2, the Lead Representatives of a New Class of des-CD Analogs of Cholecalciferol
Kutner, A.,Zhao, H.,Fitak, H.,Wilson, S. R.
, p. 22 - 32 (2007/10/02)
The design and total convergent synthesis are described for the leading representatives of the new class of analogs of cholecalciferol with the CD-ring system replaced with a two-carbon aliphatic spacer.The leading representatives of C21 retiferols (RAD1
