26738-92-1

Basic information

• Product Name: Ethanol, 2-(4-bromo-3-methylphenoxy)-
• CAS NO: 26738-92-1
• Molecular Formula: C9H11BrO2
• Molecular Weight: 231.089
• Mol File: 26738-92-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethanol, 2-(4-bromo-3-methylphenoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanol, 2-(4-bromo-3-methylphenoxy)-(26738-92-1)
• EPA Substance Registry System: Ethanol, 2-(4-bromo-3-methylphenoxy)-(26738-92-1)

Safety Data

• Hazardous Substances Data: 26738-92-1(Hazardous Substances Data)

Upstream product

• 96-49-1 [1,3]-dioxolan-2-one 
• 14472-14-1 4-bromo-3-methylphenol 
• 107-07-3 2-chloro-ethanol 

Downstream Products

• 1034685-66-9 1-bromo-2-methyl-4-[2-(tert-butyldimethylsilyloxy)ethyloxy]benzene 

Relevant articles and documents

End group-functionalization and synthesis of block-copolythiophenes by modified nickel initiators

Polythiophenes with alcohol, tosylate, azide, ethynylene, carboxylic acid, and amine end groups were prepared by a combination of functionalized nickel initiators and postpolymerization reactions. The azide and ethynylene polymers were subsequently used in a click reaction to produce a conjugated block copolymer. Finally, a conjugated triblock-copolymer was synthesized by means of a chain growth polymerization initiated by a binuclear nickel initiator.

PROCESS FOR THE PREPARATION OF 1,4,5-TRISUBSTITUTED TRIAZOLES AND 3,4,5-TRISUBSTITUTED TRIAZOLES

The present invention relates to a process for the preparation of 1,4,5- trisubstituted triazoles and 3,4,5-trisubstituted triazoles according to Formulas (Ia) and 5 (Ib), and mesomers and tautomers thereof, wherein a compound according to Formula (II) or Formula (III): is reacted with a compound according to Formula (IV). The process is very useful for the selective and site-specific addition of azide compounds to optionally activated alkynes to form 1,4,5-trisubstuted triazoles and mesomers and tautomers thereof and the application of this process to the covalent functionalisation of biomolecules.

AMINO ALCOHOL DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME, AND USE THEREOF

The present invention provides compounds represented by general formula (I): or pharmaceutical acceptable salts thereof, wherein R1 and R2 are each hydrogen or lower alkyl; R3 R4, R5 and R6 are each hydrogen, halogen, lower alkyl or lower alkoxy; R7 and R8 are each hydrogen, halogen, lower alkyl, halo-lower alkyl, lower alkoxy, cycloalkyl, aryl, heteroaryl, cyano, a hydroxyl group, lower acyl, carboxy or the like; R9 is -C(O)-R10, -A1-C(O)-R10, -O-A2-C(O)-R10 or a tetrazol-5-yl group, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.