21213-67-2 Usage
Molecular structure
The chemical 1,3-Benzodioxole,5-[[(2E)-5-(3,3-dimethyloxiranyl)3-methyl-2-pentenyl]oxy]has a complex molecular structure that includes benzene and dioxole rings, as well as a side chain derived from 3,3-dimethyloxiranyl, 3-methyl, and 2-pentenyl.
Aromatic properties
Due to its molecular structure, this chemical exhibits aromatic properties, which contribute to its use in the production of pharmaceuticals, perfumes, and flavorings.
Potential medicinal effects
The compound may have potential medicinal effects, although further research would be required to determine its specific applications in this area.
Applications in organic synthesis
The chemical may be used in organic synthesis, which involves the formation of new chemical compounds from simpler molecules.
Professional or industrial use
Before handling or using 1,3-Benzodioxole,5-[[(2E)-5-(3,3-dimethyloxiranyl)- 3-methyl-2-pentenyl]oxy]- in a professional or industrial setting, its specific uses and potential hazards should be carefully evaluated.
Safety considerations
As with any chemical compound, safety precautions should be taken when handling or using 1,3-Benzodioxole,5-[[(2E)-5-(3,3-dimethyloxiranyl)3-methyl-2-pentenyl]oxy]to minimize the risk of harm to individuals or the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 21213-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,1 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21213-67:
(7*2)+(6*1)+(5*2)+(4*1)+(3*3)+(2*6)+(1*7)=62
62 % 10 = 2
So 21213-67-2 is a valid CAS Registry Number.
21213-67-2Relevant academic research and scientific papers
Archelas,Delbecque,Furstoss
, p. 2445 - 2446 (1993)
The enantioselective epoxide biohydrolysis of the racemic benzodioxole 6,7-epoxygeraniol derivative 1 has been achieved using the fungus A. niger. This new type of preparative scale bioconversion allows the synthesis of both enantiomers of Bower's compound, an analogue of insect juvenile hormone. Biological tests showed that the 6(R) enantiomer was about ten times more active than the 6(S) enantiomer against the yellow meal worm Tenebrio molitor.
