53178-46-4 Usage
Description
1-(1,3-Dithiane-2-yl)-2-cyclohexen-1-ol is a chemical compound with the molecular formula C10H16OS. It is an alcohol derivative that contains a dithiane group and a cyclohexene ring. 1-(1,3-Dithiane-2-yl)-2-cyclohexen-1-ol is known for its reactivity as a nucleophile and a chelating agent, which makes it a versatile building block in organic chemistry.
Uses
Used in Pharmaceutical Industry:
1-(1,3-Dithiane-2-yl)-2-cyclohexen-1-ol is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique structure and reactivity allow for the creation of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(1,3-Dithiane-2-yl)-2-cyclohexen-1-ol is utilized as a synthetic intermediate for the development of agrochemicals. Its properties enable the synthesis of compounds that can be used in the production of pesticides, herbicides, and other agricultural products to improve crop yield and protect plants from pests.
Used in Material Science:
1-(1,3-Dithiane-2-yl)-2-cyclohexen-1-ol has been researched for its potential applications in material science. Its unique structure and reactivity may contribute to the development of new materials with specific properties, such as improved strength, flexibility, or chemical resistance.
Used in Catalysis:
1-(1,3-Dithiane-2-yl)-2-cyclohexen-1-ol has also been investigated for its use in catalysis, where it could potentially serve as a catalyst or a catalyst support. Its ability to act as a nucleophile and a chelating agent may enable it to facilitate various chemical reactions, leading to more efficient and environmentally friendly processes in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 53178-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,7 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53178-46:
(7*5)+(6*3)+(5*1)+(4*7)+(3*8)+(2*4)+(1*6)=124
124 % 10 = 4
So 53178-46-4 is a valid CAS Registry Number.
53178-46-4Relevant articles and documents
Substitution of HMPT by the Cyclic Urea DMPU as a Cosolvent for Highly Reactive Nucleophiles and Bases
Mukhopadhyay, Triptikumar,Seebach, Dieter
, p. 385 - 391 (1982)
The cyclic urea DMPU (N,N'-dimethyl-N,N'-propylene urea = 1,3-dimethyl-2-oxo-hexahydropyrimidine) is shown to exhibit the same effects as HMPT in oxirane-opening with Li-acetylide, in Wittig olefination, in the double deprotonation of a nitroalkane, in th
Replacement of HMPA in samarium diiodide promoted cyclizations and reactions of organolithium compounds
Berndt, Mathias,Hoelemann, Alexandra,Niermann, Andre,Bentz, Christoph,Zimmer, Reinhold,Reissig, Hans-Ulrich
experimental part, p. 1299 - 1302 (2012/04/04)
Tripyrrolidinophosphoric acid triamide (TPPA) can replace carcinogenic HMPA as a Lewis basic additive in many reactions involving samarium ketyls. In most cases, yields and selectivities of cyclizations of (het)aryl, alkenyl, and alkynyl ketones are simil
Studies on the substituted 3-aminopropan-1-ol motif of lycoctonine class norditerpenid alkaloids: A novel route to 3-hydroxymethylcyclohex-2-enone
Doisy, Xavier,Blagbrough, Ian S.,Thomas, Noel F.,Potter, Barry V. L.
, p. 8525 - 8528 (2007/10/03)
Pursuing our interest in methyllcaconitine (MLA), we have designed a synthetic route to substituted ring-A of lycoctonine class norditerpenoid alkaloids. A novel synthesis of 3-hydroxymethylcyclohex-2-enone has been achieved starting from cyclohex-2-enone. Key reactions are: 1,2-addition of 1,3-dithiane followed by allylic rearrangement, 1,4-hydrocyanation, Wittig reaction and conversion into the substituted N-ethyl-3-aminopropan-1-ol motif of these neopentyl-like alcohols.
