20061-24-9 Usage
General Description
1,1-Cyclobutanedimethanol, 3-(phenylmethoxy)- is a chemical compound with the molecular formula C12H16O6. It is a cyclobutane derivative with two hydroxyl groups and a phenylmethoxy group attached to the carbon backbone. 1,1-Cyclobutanedimethanol, 3-(phenylmethoxy)- is commonly utilized as a building block in organic synthesis and can be used in the production of various polymers and resins. It may also have potential applications in the development of pharmaceuticals and agrochemicals due to its unique structural properties. Additionally, it may be used as a reagent in chemical reactions or as a solvent in certain processes. Overall, 1,1-Cyclobutanedimethanol, 3-(phenylmethoxy)- has diverse potential uses in the fields of chemistry, materials science, and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 20061-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,6 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20061-24:
(7*2)+(6*0)+(5*0)+(4*6)+(3*1)+(2*2)+(1*4)=49
49 % 10 = 9
So 20061-24-9 is a valid CAS Registry Number.
20061-24-9Relevant articles and documents
Design and synthesis of spirocyclic compounds as HCV replication inhibitors by targeting viral NS4B protein
Tai, Vincent W.-F.,Garrido, Dulce,Price, Daniel J.,Maynard, Andrew,Pouliot, Jeffrey J.,Xiong, Zhiping,Seal, John W.,Creech, Katrina L.,Kryn, Luz H.,Baughman, Todd M.,Peat, Andrew J.
, p. 2288 - 2294 (2014/05/20)
Two novel series of spirocyclic piperidine analogs appended to a pyrazolo[1,5-a]pyridine core were designed, synthesized and evaluated for their anti-HCV activity. A series of piperidine ketals afforded dispiro 6p which showed excellent in vitro anti-HCV activities (EC50 of 1.5 nM and 1.2 nM against genotype 1a and 1b replicons, respectively). A series of piperidine oxazolidinones afforded 27c which showed EC50's of 10.9 nM and 6.1 nM against 1a and 1b replicons, respectively. Both compounds 6p and 27c bound directly to non-structural NS4B protein in vitro (IC50's = 10.2 and 30.4 nM, respectively) and exhibited reduced potency in replicons containing resistance mutations encoding changes in the NS4B protein.
Synthesis of 3-adenyl- and 3-thyminylcyclobutane-1,1-dimethanols and their homo-octameric phosphodiesters
Henlin,Rink,Spieser,Baschang
, p. 589 - 603 (2007/10/02)
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