6135-54-2

Basic information

• Product Name: 2-tert-Butyl-2-methyl-1,3-dioxolane
• Synonyms: 2-tert-Butyl-2-methyl-1,3-dioxolane
• CAS NO: 6135-54-2
• Molecular Formula: C₈H₁₆O₂
• Molecular Weight: 144.2114
• Mol File: 6135-54-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 142°Cat760mmHg
• Flash Point: 39.2°C
• Appearance: /
• Density: 0.927g/cm³
• Vapor Pressure: 7.14mmHg at 25°C
• Refractive Index: 1.426
• CAS DataBase Reference: 2-tert-Butyl-2-methyl-1,3-dioxolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-tert-Butyl-2-methyl-1,3-dioxolane(6135-54-2)
• EPA Substance Registry System: 2-tert-Butyl-2-methyl-1,3-dioxolane(6135-54-2)

Safety Data

• Hazardous Substances Data: 6135-54-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H16O2/c1-7(2,3)8(4)9-5-6-10-8/h5-6H2,1-4H3

Upstream product

• 75-97-8 3,3-dimethyl-butan-2-one 
• 107-21-1 ethylene glycol 
• 917-92-0 3,3-Dimethylbut-1-yne 

Downstream Products

• 542-59-6 2-hydroxyethyl acetate 
• 132381-82-9 5-tert-Butyl-1,2,4-Benzenetricarbonitrile 
• 58219-46-8 2-(tert-butyl)succinic acid dimethyl ester 
• 75-97-8 3,3-dimethyl-butan-2-one 
• 87-87-6 2,3,5,6-tetrachlorobenzene-1,4-diol 
• 139071-40-2 1,4-dicyano-2,5-bis(1,1-dimethylethyl)benzene 
• 139100-52-0 2,4-dicyano-1,5-bis(1,1-dimethylethyl)benzene 
• 464-07-3 3,3-dimethyl-2-butanol 
• 97419-14-2 2-(2,2,2-trifluoroethoxy)-2-methyl-1,3-dioxolane 
• 139071-39-9 5-Hexyl-1,2,4-benzenetricarbonitrile 
• 19798-71-1 2-methyl-2-methoxy-1,3-dioxolane 

Relevant articles and documents

Experimental and Theoretical Study of the Effectiveness and Stability of Gold(I) Catalysts Used in the Synthesis of Cyclic Acetals

Different [AuL]+ fragments (L = tertiary phosphines, ylides, or NHC carbene) have been tested under mild conditions as suitable catalysts for the transformation of terminal or internal alkynes into the corresponding cyclic acetals upon reaction

Radicals through Photoinduced Electron Transfer. Addition to Olefin and Addition to Olefin-Aromatic Substitution Reactions

The radical cations of 2,2-dialkyl- and 2-alkyl-2-aryl-1,3-dioxolanes, when generated in solution by photoinduced electron transfer to 1,2,4,5-benzenetetracarbonitrile (TCB), fragment to yield alkyl radicals.These are trapped by electron-withdrawing substituted alkenes (acrylonitrile, methyl acrylate, methyl vinyl ketone, as well as dimethyl maleate and fumarate).The radicals thus formed are either reduced by the TCB radical anion or add to it.In the first process (observed only with the diesters) the end result is reductive alkylation of the olefin, while the latter process results in an addition to the olefin-aromatic substitution reaction.The selectivity of the process is explained on the basis of steric hindrance, since the radicals react when still in the cage with the aromatic radical anion.