26902-25-0

Basic information

• Product Name: 2-Butene, 1,1'-oxybis[3-methyl]
• Synonyms: 2-Butene, 1,1'-oxybis[3-methyl]
• CAS NO: 26902-25-0
• Molecular Formula: C₁₀H₁₈O
• Molecular Weight: 154.25
• Mol File: 26902-25-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 55 °C(Press: 3 Torr)
• Appearance: /
• Density: 0.8380 g/cm3(Temp: 16 °C)
• CAS DataBase Reference: 2-Butene, 1,1'-oxybis[3-methyl](CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butene, 1,1'-oxybis[3-methyl](26902-25-0)
• EPA Substance Registry System: 2-Butene, 1,1'-oxybis[3-methyl](26902-25-0)

Safety Data

• Hazardous Substances Data: 26902-25-0(Hazardous Substances Data)

Upstream product

• 556-82-1 3-methyl-2-buten-1-ol 
• 115-18-4 2-methyl-3-buten-2-ol 
• 7647-01-0 hydrogenchloride 
• 78-39-7 Triethyl orthoacetate 
• 1445-45-0 Trimethyl orthoacetate 
• 123-31-9 hydroquinone 
• 106-44-5 p-cresol 

Downstream Products

• 544-01-4 isopentyl ether 
• 27644-04-8 (+-)-artemisia alcohol 
• 763-32-6 2-methyl-1-buten-4-ol 
• 58461-27-1 (+/-)-lavandulol 
• 123-51-3 i-Amyl alcohol 
• 78-78-4 methylbutane 
• 5392-40-5 (E/Z)-3,7-dimethyl-2,6-octadienal 

Relevant articles and documents

Prenylation of 4-Methylphenol

Abstract: Organoaluminum (aluminum phenolate and aluminum isopropylate) and acidicheterogeneous catalysts (zeolites C-10, C-100 and ZSM, clay KSF, sulfonic cationexchangers Fiban K-1 and Amberlist 36 Dry) were studied in the alkylation of4-methylphenol wi

Reaction of orthoesters with alcohols in the presence of acidic catalysts: A study

Allylic and benzylic alcohols are converted into corresponding unsymmetrical ethers when reacted with various orthoesters in the presence of montmorillonite KSF at ambient temperature. A detailed study has been undertaken to examine the mechanism and generality of these reactions with regard to various acidic catalysts, which reveal interesting competitive reactions mainly O-acetylation, together with trace amount of dimerized product. The type of the side product and their relative quantity depends upon the nature of the catalyst employed. Furthermore, the low yields of the Claisen rearrangement product obtained from allylic alcohols under heating is rationalized due to the formation of some of these products.

Cetonisation catalytique du methyl-2-butene-3-ol par des complexes du rhodium(III) ou du palladium(II)

A number of efficient catalytic procedures for the oxidation of acid-sensitive substrate such as 2-methyl-3-buten-2-ol to the corresponding ketone (2-methyl-butan-2-ol-3-one) are compared.Reaction with dioxygen (or quinone) and a palladium precursor (PdCl2 or ) under mild conditions (=35 deg C), gave good conversions (98percent) and good selectivities (=90percent).