1129-64-2

Basic information

• Product Name: Benzene, (3-methylbutoxy)-
• CAS NO: 1129-64-2
• Molecular Formula: C11H16O
• Molecular Weight: 164.247
• Mol File: 1129-64-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, (3-methylbutoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (3-methylbutoxy)-(1129-64-2)
• EPA Substance Registry System: Benzene, (3-methylbutoxy)-(1129-64-2)

Safety Data

• Hazardous Substances Data: 1129-64-2(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 19533-24-5 sodium isopentoxide 
• 2684-02-8 benzenediazonium 
• 123-51-3 i-Amyl alcohol 
• 934-55-4 potassium benzenesulfonate 
• 107-84-6 1-chloro-3-methylbutane 
• 139-02-6 sodium phenoxide 
• 541-28-6 isopentyl iodide 
• 100-67-4 potassium phenolate 
• 108-95-2 phenol 
• 64-17-5 ethanol 
• 14309-15-0 phenyl prenyl ether 
• 107-82-4 i-pentyl bromide 
• 108-94-1 cyclohexanone 

Downstream Products

• 503-74-2 3-methylbutyric acid 
• 15719-64-9 methylammonium carbonate 
• 106-51-4 p-benzoquinone 
• 160127-64-0 1-iodo-4-(isopentyloxy)benzene 
• 1163-68-4 2-<4-Isopentoxy-phenylmercaptomethyl>-benzoesaeure 
• 95962-03-1 N⁴-<2-(4-Isopentyloxy-benzoyl)-ethyl>-N¹-butylcarbamoyl-sulfanilamid 
• 14794-54-8 N-Hydroxy-2-[4-(3-methyl-butoxy)-phenyl]-acetamide 
• 18986-09-9 4-(3-methylbutoxy)benzaldehyde 
• 664326-22-1 but-2-enedioic acid bis{2,2-bis[4-(3-methylbutoxy)phenyl]ethylamide} 
• 664326-25-4 bis[4-(3-methylbutoxy)phenyl]acetamide 
• 664326-26-5 2,2-bis[4-(3-methylbutoxy)phenyl]ethylamine 
• 664326-24-3 bis[4-(3-methylbutoxy)phenyl]acetic acid 
• 15560-77-7 [4-(3-Methyl-butoxy)-phenyl]-acetic acid ethyl ester 
• 1141-92-0 4-isopentyloxy-benzenesulfonic acid amide 

Relevant articles and documents

Straightforward heterogeneous palladium catalyzed synthesis of aryl ethers and aryl amines via a solvent free aerobic and non-aerobic dehydrogenative arylation

Aryl ethers have been prepared from cyclohexanone derivatives and various alcohols in the presence of a catalytic amount of palladium on charcoal. The formation of an enol ether followed by an aerobic or non-aerobic dehydrogenation reaction, seem to be the key steps of this transformation. In addition, this new method was also adapted for the synthesis of arylamines.

PHENYLATION OF PRIMARY AND SECONDARY ALCOHOLS WITH THE TRIPHENYLBISMUTHINE-COPPER DIACETATE SYSTEM

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REACTION OF TRIPHENYLBISMUTH WITH COPPER DIACETATE IN THE PRESENCE OF ALCOHOLS

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