342644-91-1 Usage
Uses
Used in Pharmaceutical Applications:
[3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-(3-hydroxypropoxy)-2-methylenecyclohexylidene]ethanol is used as a potential pharmaceutical compound for its unique molecular structure and functional groups. The presence of multiple hydroxyl groups may allow for interactions with biopolymers and macromolecules, making it a candidate for drug development and therapeutic applications.
Used in Chemical Synthesis:
In the chemical industry, [3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-(3-hydroxypropoxy)-2-methylenecyclohexylidene]ethanol can be used as a starting material or intermediate in the synthesis of other complex organic compounds. Its specific stereochemistry and functional groups may be exploited to create novel molecules with desired properties.
Used in Research and Development:
[3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-(3-hydroxypropoxy)-2-methylenecyclohexylidene]ethanol may also be utilized in research and development settings to study its properties, reactivity, and potential applications. The intricate structure and specific stereochemistry of [3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-(3-hydroxypropoxy)-2-methylenecyclohexylidene]ethanol make it an interesting subject for scientific investigation and potential innovation in various fields.
Used in Material Science:
In material science, [3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-(3-hydroxypropoxy)-2-methylenecyclohexylidene]ethanol could be explored for its potential to create new materials with unique properties, such as improved strength, flexibility, or chemical resistance, depending on its reactivity and compatibility with other materials.
Used in Cosmetics Industry:
[3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-(3-hydroxypropoxy)-2-methylenecyclohexylidene]ethanol may also find applications in the cosmetics industry, where its unique structure and functional groups could be leveraged to develop new formulations with enhanced properties, such as improved skin hydration, texture, or appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 342644-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,6,4 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 342644-91:
(8*3)+(7*4)+(6*2)+(5*6)+(4*4)+(3*4)+(2*9)+(1*1)=141
141 % 10 = 1
So 342644-91-1 is a valid CAS Registry Number.
342644-91-1Relevant academic research and scientific papers
Parallel synthesis of a vitamin D3 library in the solid-phase
Hijikuro,Doi,Takahashi
, p. 3716 - 3722 (2007/10/03)
A highly efficient synthesis of the vitamin D3 system on solid support is described. Two synthetic strategies for the solid-phase synthesis of vitamin D3 were developed. One is for 11-hydroxy analogues, and the other is for most other synthetic analogues. In the latter strategy, the sulfonate-linked CD-ring 58 was initially immobilized on PS-DES resin to give solid-supported CD-ring 63 (Scheme 10). Similarly, solid-supported CD-ring 63 was prepared by attachment of the CD-ring 10 to the chlorosulfonate resin 64. The vitamin D3 system was synthesized by Horner-Wadsworth-Emmons reaction of the A-ring phosphine oxide to a solid-supported CD-ring, followed by simultaneous introduction of the side chain and cleavage from resin with a Cu1-catalyzed Grignard reagent. Parallel synthesis of the vitamin D3 analogues was accomplished by a split and pool methodology utilizing radio frequency encoded combinatorial chemistry, and a manual parallel synthesizer for side chain diversification and deprotection. Additionally, we demonstrated the synthesis of various A-rings in a similar protocol for efficient preparation of building blocks.
