182-55-8 Usage
General Description
Spiro[1,3-benzodioxole-2,1'-cyclohexane] is a chemical compound derived from the combination of spiro compounds which are a class of organic compounds characterized by atoms fixed in a spiral orientation, benzodioxole which is a type of ether and a cyclic ether containing a benzene ring and cyclohexane, which is a cycloalkane. The resulting compound is stable and has properties similar to both benzodioxole and cyclohexane. Although its specific uses and applications are not widely documented, like many other organic compounds, it may be of interest in chemical research, pharmaceutical manufacturing or industrial settings. As with all chemicals, proper handling, storage and disposal should be practiced to prevent harmful exposure and environmental impact. Further research is needed to understand the properties and applications of spiro[1,3-benzodioxole-2,1'-cyclohexane] more comprehensively.
Check Digit Verification of cas no
The CAS Registry Mumber 182-55-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,8 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 182-55:
(5*1)+(4*8)+(3*2)+(2*5)+(1*5)=58
58 % 10 = 8
So 182-55-8 is a valid CAS Registry Number.
182-55-8Relevant articles and documents
Copper-Catalyzed Asymmetric Three-Component Borylstannation: Enantioselective Formation of C-Sn Bond
Jia, Tao,Cao, Peng,Wang, Ding,Lou, Yazhou,Liao, Jian
, p. 4918 - 4922 (2015)
In summary, a first copper-catalyzed synthesis of α-aryl-β-borylstannane compounds was accomplished through three-component borylstannation of aryl-substituted alkenes. In the exploration of an asymmetric variant, chiral sulfinylphosphine ligands proved a
Cu(II)-impregnated sulfated MCM-41: An efficient and convenient protocol for the synthesis of 1,3-benzodioxoles
Sivakumar,Ramesh,Lalitha
experimental part, p. 91 - 93 (2011/03/23)
An efficient synthesis of 1,3-benzodioxoles was achieved from catechol with different aldehydes and ketones using Cu(II) impregnated sulfated MCM-41 as an efficient and reusable catalyst. Copyright Taylor & Francis Group, LLC.
Diallylation of 2,2-dialkylbenzodioxoles from TiCl4-mediated allylsilane reaction
Galy, Nicolas,Moraleda, Delphine,Santelli, Maurice
body text, p. 5238 - 5240 (2009/12/06)
Reaction of aliphatic ketones with catechol afforded 2,2-dialkylbenzodioxoles. Treatment of these benzodioxoles with allyltrimethylsilane in the presence of titanium tetrachloride led to 4,4-dialkylhepta-1,6-dienes resulting from a diallylation process. R
