147725-62-0 Usage
Description
(1S)-1-((1S,3aR,7aR)-4-(tert-butyldimethylsilyloxy)-7a-methyloctahydro-1H-inden-1-yl)ethanol is a complex chemical compound with a chiral structure and a functional group consisting of a tert-butyldimethylsilyloxy moiety. It is commonly used as an intermediate or building block in organic synthesis.
Uses
Used in Pharmaceutical Industry:
(1S)-1-((1S,3aR,7aR)-4-(tert-butyldimethylsilyloxy)-7a-methyloctahydro-1H-inden-1-yl)ethanol is used as a chiral intermediate for the synthesis of pharmaceutical compounds. Its chiral structure and functional group make it suitable for the development of enantioselective reactions and the production of chiral drugs.
Used in Agrochemical Industry:
(1S)-1-((1S,3aR,7aR)-4-(tert-butyldimethylsilyloxy)-7a-methyloctahydro-1H-inden-1-yl)ethanol is used as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its functional group allows for the attachment of various chemical moieties to create new agrochemical compounds.
Used in Materials Science:
(1S)-1-((1S,3aR,7aR)-4-(tert-butyldimethylsilyloxy)-7a-methyloctahydro-1H-inden-1-yl)ethanol is used as a precursor for the development of new materials with specific properties. Its functional group can be utilized for the synthesis of polymers, coatings, and other materials with tailored characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 147725-62-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,7,2 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 147725-62:
(8*1)+(7*4)+(6*7)+(5*7)+(4*2)+(3*5)+(2*6)+(1*2)=150
150 % 10 = 0
So 147725-62-0 is a valid CAS Registry Number.
147725-62-0Relevant articles and documents
VITAMIN D RECEPTOR ACTIVATORS AND METHODS OF MAKING
-
Page/Page column 24, (2009/05/28)
The invention relates to compounds that are vitamin D receptor activators, compositions comprising such compounds, methods of using such compounds and compositions, processes for preparing such compounds, and intermediates obtained during such processes.
Synthesis of novel hapten derivatives of 1α,25-dihydroxyvitamin D3 and its 20-epi analogue
Blaehr, Lars K. A.,Bjoerkling, Fredrik,Calverley, Martin J.,Binderup, Ernst,Begtrup, Mikael
, p. 1367 - 1375 (2007/10/03)
Hapten derivatives of 1α,25-dihydroxyvitamin D3 and its 20-epimer were synthesized and conjugated to a carrier protein for raising polyclonal antibodies. The haptens were linked through spacers at C-16, thereby exposing both the A-ring and the side chain of the molecules, to maximize antibody specificity. The spacers were introduced via stereoselective hydroboration of 16-ene intermediates as the key step. In immunoassays, the antibodies raised toward the natural hormone were selective to this compound over derivatives with modifications in the A-ring or the side chain. The antibodies toward the 20-epimer, however, were unable to recognize modifications in the side chain.
A new approach to the synthesis of the 25-hydroxy-22-oxa-vitamin D3 side chain
Fall, Yagamare
, p. 4909 - 4912 (2007/10/03)
An efficient new method is described for the construction of the 25-hydroxy-22-oxavitamin D3 side-chain, which is present in several analogues of calcitriol with antitumour activity.
