34678-64-3

Basic information

• Product Name: 1,2-bis(2-methylpropyloxy)benzene
• Synonyms: 1,2-bis(2-methylpropyloxy)benzene
• CAS NO: 34678-64-3
• Molecular Weight: 222.327
• Mol File: 34678-64-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,2-bis(2-methylpropyloxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-bis(2-methylpropyloxy)benzene(34678-64-3)
• EPA Substance Registry System: 1,2-bis(2-methylpropyloxy)benzene(34678-64-3)

Safety Data

• Hazardous Substances Data: 34678-64-3(Hazardous Substances Data)

Upstream product

• 20244-21-7 sodium catecholate 
• 78-77-3 Isobutyl bromide 
• 513-38-2 Isobutyl iodide 
• 120-80-9 benzene-1,2-diol 
• 513-36-0 isobutyryl chloride 
• 10500-86-4 1,2-bis(β-methallyloxy)benzene 

Downstream Products

• 5542-71-2 3,4-Diisobutoxy-nitrobenzol 
• 57596-02-8 3-(3,4-dihydroxybenzoyl)propionic acid 
• 288574-54-9 1,2-diisobutoxy-4-iodobenzene 

Relevant articles and documents

Substituent effect on iron phthalocyanines as cyclohexene oxidation catalysts

Two iron phthalocyanines peripherally octasubstituted either with electron-withdrawing isobutylsulfonyl moities or electron-donating isobutoxy moieties were designed to investigate the effect of the substitution pattern on their oxidation catalytic activi

Polymer electroluminescent device

A polymer electroluminescent device (1) comprises an electroluminescent layer (7) of a poly(1,4-phenylenevinylene) having aryl-1,4-phenylene units, where the aryl group is a phenyl, naphthyl or biphenylyl group. Using such a poly(1,4-phenylenevinylene) has the effect that the light emitted by the polymer electroluminescent device has no or at least a reduced tendency to change color when driven the device is and/or kept at an elevated ambient temperature of, for example, 70 °C. The poly(1,4-phenylenevinylene)s having aryl-1,4-phenylene units are prepared using aryl-bishalomethylbenzenes as an intermediate compound.

PHOSPHORORGANISCHE VERBINDUNGEN 101. TERTIAERE PHOSPHINE MIT ORTHOALKOXYPHENYL-GRUPPEN. Synthese und Eigenschaften

Alkylphenylethers, ortho-lithiated in good yields, are transformed according to scheme (1) to the triarylphosphines ArPPh2, Ar2PPh and Ar3P (Ar contains in all cases an ortho-alkoxy group) (Table 1.).Hydroquinonedialkylethers can be lithiated twice, forming the compounds 102 and 103.Table 2 summarizes some arylalkylethers (71 - 101) which were lithiated; table 7 presents 12 new arylalkylethers.The syntheses of triarylphosphines with one or two bulky groups (105 - 110) and of triarylphosphines with one or two 3,4-dialkoxyphenyl groups (111 - 114) are reported.The 31P-spectra of the compounds prepared are discussed with respect to the validity of the Tolman-rule.