112670-78-7 Usage
Description
(1S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-methylene-3-[2-[(1R,3aS)-7a-methyl-1-((E)-(1R,4R)-1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-(4E)-ylidene]-eth-(E)-ylidene]-cyclohexanol is a complex chiral molecule with a cyclohexane ring as its main structural backbone. It contains multiple functional groups, including a silanol group, a double bond, and a hydroxyl group. (1S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-methylene-3-[2-[(1R,3aS)-7a-methyl-1-((E)-(1R,4R)-1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-(4E)-ylidene]-eth-(E)-ylidene]-cyclohexanol also features a trimethyl-hexenyl group and an octahydro-indenylidene group, which contribute to its unique and intricate molecular structure. This chemical may have potential applications in various fields, such as organic synthesis, pharmaceuticals, or materials science.
Uses
Used in Organic Synthesis:
(1S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-methylene-3-[2-[(1R,3aS)-7a-methyl-1-((E)-(1R,4R)-1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-(4E)-ylidene]-eth-(E)-ylidene]-cyclohexanol is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique molecular structure allows for selective reactions and the formation of new chemical bonds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-methylene-3-[2-[(1R,3aS)-7a-methyl-1-((E)-(1R,4R)-1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-(4E)-ylidene]-eth-(E)-ylidene]-cyclohexanol is used as a potential drug candidate or as a building block for the development of new pharmaceutical compounds. Its chiral nature and functional groups can be exploited to create molecules with specific biological activities and therapeutic effects.
Used in Materials Science:
(1S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-methylene-3-[2-[(1R,3aS)-7a-methyl-1-((E)-(1R,4R)-1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-(4E)-ylidene]-eth-(E)-ylidene]-cyclohexanol is used in materials science for the development of new materials with unique properties. Its molecular structure can be utilized to create novel polymers, coatings, or other materials with specific characteristics, such as improved stability, reactivity, or selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 112670-78-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,7 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112670-78:
(8*1)+(7*1)+(6*2)+(5*6)+(4*7)+(3*0)+(2*7)+(1*8)=107
107 % 10 = 7
So 112670-78-7 is a valid CAS Registry Number.
112670-78-7Relevant 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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