104846-63-1 Usage
Description
tert-butyl((E)-3-((E)-2-((1R,3aS,7aR)-1-((2R,5R,E)-5,6-diMethylhept-3-en-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-4-Methylenecyclohexyloxy)diMethylsilane is a complex organic compound with a unique molecular structure. It is characterized by a tert-butyl group, an (E)-3-((E)-2-((1R,3aS,7aR)-1-((2R,5R,E)-5,6-diMethylhept-3-en-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-4-Methylenecyclohexyloxy)dimethylsilyl group, and a light yellow oil appearance.
Uses
1. Used in Chemical Synthesis:
tert-butyl((E)-3-((E)-2-((1R,3aS,7aR)-1-((2R,5R,E)-5,6-diMethylhept-3-en-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-4-Methylenecyclohexyloxy)diMethylsilane is used as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for selective reactions and functional group transformations, making it a valuable building block in organic synthesis.
2. Used in Material Science:
In the field of material science, tert-butyl((E)-3-((E)-2-((1R,3aS,7aR)-1-((2R,5R,E)-5,6-diMethylhept-3-en-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-4-Methylenecyclohexyloxy)diMethylsilane is utilized as a precursor for the development of novel materials with specific properties. Its ability to form stable complexes and its compatibility with various polymers make it suitable for creating advanced materials with improved performance characteristics.
3. Used in Analytical Chemistry:
tert-butyl((E)-3-((E)-2-((1R,3aS,7aR)-1-((2R,5R,E)-5,6-diMethylhept-3-en-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-4-Methylenecyclohexyloxy)diMethylsilane can be employed as a chiral derivatizing agent in analytical chemistry. Its ability to selectively react with enantiomers can be used to differentiate between them, allowing for the accurate determination of their concentrations in various samples.
4. Used in Photochemistry:
In photochemistry, tert-butyl((E)-3-((E)-2-((1R,3aS,7aR)-1-((2R,5R,E)-5,6-diMethylhept-3-en-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-4-Methylenecyclohexyloxy)diMethylsilane can be used as a photosensitizer or a photoinitiator in various photochemical reactions. Its ability to absorb light and generate reactive species can be harnessed to drive chemical transformations under mild conditions.
5. Used in Environmental Applications:
tert-butyl((E)-3-((E)-2-((1R,3aS,7aR)-1-((2R,5R,E)-5,6-diMethylhept-3-en-2-yl)
Check Digit Verification of cas no
The CAS Registry Mumber 104846-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,4 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104846-63:
(8*1)+(7*0)+(6*4)+(5*8)+(4*4)+(3*6)+(2*6)+(1*3)=121
121 % 10 = 1
So 104846-63-1 is a valid CAS Registry Number.
104846-63-1Relevant articles and documents
Synthesis of 24(28)-methylene-1α-hydroxyvitamin D3, a novel vitamin D3 analogue
Guo, Wei,Fang, Zhijie,Li, Hongliang,Liu, Yanan
, p. 231 - 235 (2014/05/06)
24(28)-Methylene-1α-hydroxyvitamin D3 was synthesised in 13 steps from vitamin D2. The key step of the synthesis involved the Wittig-Horner olefination of a nor-vitamin D2 aldehyde with diethylphosphono-3-methyl-2-butanone
Synthesis of a Biologically Active Vitamine-D2 Metabolite
Choudhry, Satish C.,Belica, Peter S.,Coffen, David L.,Focella, Antonino,Maehr, Hubert,et al.
, p. 1496 - 1500 (2007/10/02)
The synthesis of 1α,25,28-trihydroxyvitamin-D2 (1) from vitamin-D2 is described.Approaches to the upper side-chain synthon via the chiral sulfone 15, prepared either through the enzymatic resolution of 10 or the opening of the optica
Synthesis of MC 903, a biologically active vitamin D metabolite analogue
Calverley
, p. 4609 - 4619,4609-4619 (2007/10/02)
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