22428-86-0 Usage
Description
1,4-Dithiaspiro[4.5]decan-8-ol is a unique chemical compound characterized by its molecular formula C8H16OS2. This colorless to light yellow liquid possesses a molecular weight of 184.34 g/mol and features an eight-membered spirocyclic ring with two sulfur atoms and a hydroxyl group attached. Its distinctive structure makes it a valuable component in various research and industrial applications.
Uses
Used in Pharmaceutical Manufacturing:
1,4-Dithiaspiro[4.5]decan-8-ol is utilized as a key component in the production of pharmaceuticals, contributing to the development of new drugs and medicines. Its unique structure allows it to serve as a building block for the synthesis of various therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 1,4-Dithiaspiro[4.5]decan-8-ol is employed as a versatile building block. Its distinctive spirocyclic ring and sulfur atoms make it a valuable precursor for the creation of complex organic molecules and compounds, further expanding its applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 22428-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,2 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22428-86:
(7*2)+(6*2)+(5*4)+(4*2)+(3*8)+(2*8)+(1*6)=100
100 % 10 = 0
So 22428-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H14OS2/c9-7-1-3-8(4-2-7)10-5-6-11-8/h7,9H,1-6H2
22428-86-0Relevant articles and documents
Origin of stereocontrol in the construction of the 12-oxatricyclo[6.3.1. 02,7]dodecane ring system by Prins-pinacol reactions
Overman, Larry E.,Tanis, Paul S.
supporting information; experimental part, p. 455 - 463 (2010/03/25)
(Chemical Equation Presented) Polycyclic products containing the 12-oxatricyclo[6.3.1.02,7]dodecane moiety having either the trans (8a-e) or cis (9a-e) relative configuration of the oxacyclic bridge and the cis angular substituents are formed s
An Investigation on Desilylation of Alkyl and Phenolic Silyl Ethers Using FeCl3
Saravanan, Parthasarathy,Singh, Vinod K.
, p. 565 - 567 (2007/10/03)
A variety of alkyl and phenolic TBDMS ethers have been efficiently cleaved using anhydrous FeCl3 in MeOH under mild conditions. It was found that choice of solvent is crucial for the rate of the deprotection of TBDMS ether with FeCl3.
Annulation of α-Formyl α,β-Unsaturated Ketones by a Michael Addition-Cyclization Sequence. A Versatile Synthesis of Alicyclic Six-Membered Rings.
Meyer, Walter L.,Brannon, Michael J.,Burgos, Celmira da G.,Goodwin, Thomas E.,Howard, Ralph W.
, p. 438 - 447 (2007/10/02)
The potential generality of the annulation sequence shown in Scheme II (10 -> 11 -> 12 -> 13 -> 14/15) has been examined in model systems.Dehydrogenation of α-formylcyclohexanones 11a-d with 1 equiv of DDQ rapidly produces α,β-unsaturated α-formyl ketones
