2,2-Dimethyl-1,3-benzodioxole, with the CAS number 14005-14-2, is an organic compound characterized by its unique dioxole structure fused with a benzene ring. This compound features two methyl groups attached to the dioxole moiety, which contributes to its chemical stability and influences its reactivity. It is typically a colorless to pale yellow liquid with a distinctive aromatic odor. The presence of the dioxole ring imparts certain polar characteristics, making it soluble in organic solvents while exhibiting limited solubility in water. 2,2-Dimethyl-1,3-benzodioxole is often studied for its potential applications in organic synthesis and as a building block in the development of various chemical compounds. Its structural features may also suggest potential biological activity, although specific pharmacological properties would require further investigation. Safety data indicates that, like many organic compounds, it should be handled with care, utilizing appropriate safety measures to avoid inhalation or skin contact.

2,2-Dimethyl-1,3-benzodioxole

14005-14-2: 1,2-(Isopropylidenedioxy)Benzene, 2,2-Dimethyl-1,3-Benzodioxazole, 2,2-Dimethyl-1,3-Benzodioxole, 98.0+%(Gc)

2,2-Dimethyl-1,3-benzodioxole is a synthetic chemical that is used in the industrial production of acetonitrile. It can be synthesized from benzene and diethyl etherate. The reaction proceeds via an electrophilic addition to the double bond followed by a protonation step. The activated 2,2-dimethyl-1,3-benzodioxole reacts with benzene to produce 3 products: phenylacetaldehyde, acetophenone, and acetone. The reaction selectivity depends on the type of solvent used and its polarity.

CAS 14005-14-2: 2,2-Dimethyl-1,3-benzodioxole

2,2-Dimethyl-1,3-benzodioxole

Ref: 54-OR922649

2,2-Dimethyl-1,3-benzodioxole

Ref: 3D-FD10072

2,2-Dimethyl-1,3-benzodioxole

Ref: 3B-D3421

2,2-Dimethylbenzo[d][1,3]dioxole

Ref: 10-F319493

1,3-Benzodioxole, 2,2-dimethyl-

Ref: IN-DA001BYG