1067185-91-4 Usage
Uses
Used in Environmental Research:
(R)-2,2-dimethyl-6-(oxiran-2-yl)-4H-benzo[d][1,3]dioxine is used as a subject of study in environmental research for understanding its toxicological effects and potential impact on ecosystems. (R)-2,2-dimethyl-6-(oxiran-2-yl)-4H-benzo[d][1,3]dioxine's presence as an environmental pollutant necessitates careful handling and disposal to prevent contamination.
Used in Chemical Waste Management:
In the chemical waste management industry, (R)-2,2-dimethyl-6-(oxiran-2-yl)-4H-benzo[d][1,3]dioxine is used as a hazardous chemical that requires special attention during waste disposal processes. Proper disposal methods are crucial to minimize the risk of environmental contamination from (R)-2,2-dimethyl-6-(oxiran-2-yl)-4H-benzo[d][1,3]dioxine.
Used in Toxicology Studies:
(R)-2,2-dimethyl-6-(oxiran-2-yl)-4H-benzo[d][1,3]dioxine serves as a test subject in toxicology studies to evaluate its effects on living organisms and to determine the potential health risks associated with exposure to (R)-2,2-dimethyl-6-(oxiran-2-yl)-4H-benzo[d][1,3]dioxine. These studies are essential for developing safety guidelines and regulations for handling and disposing of this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 1067185-91-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,7,1,8 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1067185-91:
(9*1)+(8*0)+(7*6)+(6*7)+(5*1)+(4*8)+(3*5)+(2*9)+(1*1)=164
164 % 10 = 4
So 1067185-91-4 is a valid CAS Registry Number.
1067185-91-4Relevant academic research and scientific papers
Enantioselective synthesis of phenyl-ethanolamines through application of chiral sulfoxide
Sivakumar, Aathimanivelu V.,Lahoti, Anand M.,Bhat, Sujata V.
experimental part, p. 3338 - 3347 (2011/03/19)
Efficient enantioselective synthesis of (R)- and (S)-enantiomers of 2-(tert-butylamino)-1-(p-methoxyphenyl)-ethanol has been achieved in high enantiomeric excess by using asymmetric sulfoxide as a chiral auxiliary. The present synthetic approach was further extended to the asymmetric synthesis of (R)-salbutamol. Copyright Taylor & Francis Group, LLC.
A convenient synthesis of (R)-salmeterol via Rh-catalyzed asymmetric transfer hydrogenation
Liu, Juntao,Zhou, Di,Jia, Xian,Huang, Ling,Li, Xingshu,Chan, Albert S.C.
, p. 1824 - 1828 (2008/12/22)
(R)-Salmeterol was synthesized in eight steps with salicaldehyde as the starting material. The key chiral intermediate, alcohol 5, was prepared via Rh-catalyzed asymmetric transfer hydrogenation with (S,S)-PEG-BsDPEN or (S,S)-TsDPEN ligand and sodium formate as the hydrogen donor under mild conditions.
