182250-70-0 Usage
Uses
Used in Organic Synthesis:
3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL is used as a building block in organic synthesis for its ability to contribute to the creation of various functional organic compounds, enhancing the structural and functional diversity of synthesized products.
Used in Pharmaceutical Research:
In pharmaceutical research, 3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL is used as a key intermediate for the development of new drugs, leveraging its potential biological activities to contribute to drug discovery and the advancement of medicinal chemistry.
Used in Drug Discovery and Development:
3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL is employed in drug discovery and development due to its potential biological activities, which make it a candidate for further exploration and potential incorporation into new therapeutic agents.
Used in Materials Science:
3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL is used in materials science for its potential applications in the development of new materials, taking advantage of its unique structural properties to improve material performance.
Used in Nanotechnology:
In nanotechnology, 3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL is utilized for its potential to contribute to the design and synthesis of nanoscale materials and devices, where its specific chemical and physical properties can be harnessed at the nanoscale.
Check Digit Verification of cas no
The CAS Registry Mumber 182250-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,2,5 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 182250-70:
(8*1)+(7*8)+(6*2)+(5*2)+(4*5)+(3*0)+(2*7)+(1*0)=120
120 % 10 = 0
So 182250-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C39H44O3Si2/c1-38(2,3)43(34-19-11-7-12-20-34,35-21-13-8-14-22-35)41-32-27-31(30-40)28-33(29-32)42-44(39(4,5)6,36-23-15-9-16-24-36)37-25-17-10-18-26-37/h7-29,40H,30H2,1-6H3
182250-70-0Relevant articles and documents
A simple method for controlling dendritic architecture and diversity: A parallel monomer combination approach
Freeman,Chrisstoffels,Frechet
, p. 7612 - 7617 (2007/10/03)
A novel parallel monomer combination approach to manipulating the architectural disposition of dendritic macromolecules is described. It harnesses the synthetic speed and power of the double-stage convergent growth approach and classical parallel synthesi
Alternative convergent and accelerated double-stage convergent approaches towards functionalized dendritic polyethers
Forier,Dehaen
, p. 9829 - 9846 (2007/10/03)
Alternative convergent synthesis strategies for the preparation of dendritic macromolecules, using either mesylate activation or the Mitsunobu reaction, are described. The synthesis can be further accelerated by using a double stage convergent approach. T
A fast double-stage convergent synthesis of dendritic polyethers
L'abbe, Gerrit,Forier, Bart,Dehaen, Wim
, p. 2143 - 2144 (2007/10/03)
Two tert-butyldiphenylsilyl-protected synthons 7 and 9 are prepared in excellent yields and used in a one-pot synthesis of higher generation polyether dendrons.
