200636-50-6 Usage
Description
[3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-[3-[(1,1-dimethylethyl)dimethylsilyloxy]propoxy]-2-methylenecyclohexylidene]-1-chloroethane is a complex organic compound characterized by its intricate molecular structure. It features a chloroethane group, a cyclohexylidene ring, and multiple silyloxy functional groups connected through a network of carbon-carbon and carbon-oxygen bonds. [3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-[3-[(1,1-dimethylethyl)dimethylsilyloxy]propoxy]-2-methylenecyclohexylidene]-1-chloroethane's unique structure suggests potential applications in various fields, including organic synthesis, pharmaceuticals, and materials science.
Uses
Used in Organic Synthesis:
[3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-[3-[(1,1-dimethylethyl)dimethylsilyloxy]propoxy]-2-methylenecyclohexylidene]-1-chloroethane is used as a building block for the synthesis of more complex organic molecules. Its diverse functional groups and unique stereochemistry make it a valuable starting material for creating novel compounds with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-[3-[(1,1-dimethylethyl)dimethylsilyloxy]propoxy]-2-methylenecyclohexylidene]-1-chloroethane is used as an intermediate in the development of new drugs. Its structural complexity and functional group diversity allow for the creation of potential therapeutic agents with targeted biological activities.
Used in Materials Science:
[3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-[3-[(1,1-dimethylethyl)dimethylsilyloxy]propoxy]-2-methylenecyclohexylidene]-1-chloroethane is used as a component in the development of advanced materials. Its unique molecular structure can contribute to the creation of materials with specific properties, such as improved mechanical strength, thermal stability, or chemical resistance, depending on the intended application.
Used in Chemical Research:
In the field of chemical research, [3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-[3-[(1,1-dimethylethyl)dimethylsilyloxy]propoxy]-2-methylenecyclohexylidene]-1-chloroethane serves as a model compound for studying reaction mechanisms, stereoselectivity, and the influence of functional groups on reactivity. Its complex structure provides a challenging and interesting subject for researchers to explore and understand.
Check Digit Verification of cas no
The CAS Registry Mumber 200636-50-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,6,3 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 200636-50:
(8*2)+(7*0)+(6*0)+(5*6)+(4*3)+(3*6)+(2*5)+(1*0)=86
86 % 10 = 6
So 200636-50-6 is a valid CAS Registry Number.
200636-50-6Relevant articles and documents
Two convergent approaches to the synthesis of 1,25-dihydroxy 2-(3-hydroxypropoxy)vitamin D3 (ED-71) by the lythgoe and thf trost coupling reactions
Maeyama, Junji,Hiyamizu, Hiroko,Takahashi, Keisuke,Ishihara, Jun,Hatakeyama, Susumi,Kubodera, Noboru
, p. 295 - 307 (2008/04/18)
Two convergent syntheses of 1,25-dihydroxy-2-(3-hydroxypropoxy)vitamin D3 (ED-71) by the Lythgoe coupling reaction between the A-ring phosphine oxide and the C/D-ring ketone and the Trost coupling reaction between the A-ring ene-yne and the C/D-ring bromomethylene are described.
Convergent synthesis of 1α,25-dihydroxy-2β-(3-hydroxypropoxy)vitamin D3 (ED-71)
Hatakeyama, Susumi,Ikeda, Tatsuhiko,Maeyama, Junji,Esumi, Tomoyuki,Iwabuchi, Yoshiharu,Irie, Hiroshi,Kawase, Akira,Kubodera, Noboru
, p. 2871 - 2874 (2007/10/03)
A convergent and versatile synthesis of the potent vitamin D analog, 1α,25-dihydroxy-2β-(3-hydroxypropoxy)vitamin D3 [1] (ED-71) is described.
