3233-03-2

Basic information

• Product Name: 2-Propanol, 1-(methylphenylamino)-
• CAS NO: 3233-03-2
• Molecular Formula: C10H15NO
• Molecular Weight: 165.235
• Mol File: 3233-03-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Propanol, 1-(methylphenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propanol, 1-(methylphenylamino)-(3233-03-2)
• EPA Substance Registry System: 2-Propanol, 1-(methylphenylamino)-(3233-03-2)

Safety Data

• Hazardous Substances Data: 3233-03-2(Hazardous Substances Data)

Upstream product

• 87-72-9 D-Xylose 
• 73-34-7 6-deoxy-L-galactose 
• 100-61-8 N-methylaniline 
• 75-56-9 methyloxirane 
• 127-00-4 1-Chloro-2-propanol 

Downstream Products

• 15885-06-0 1-[methyl(phenyl)amino]propan-2-one 
• 15973-76-9 N-(2-bromopropyl)-N-methylaniline 
• 1604039-11-3 N-(2-iodopropyl)-N-methylaniline 
• 1604039-72-6 N-methyl-N-(2,5,5-trimethylhex-3-yn-1-yl)aniline 
• 73861-82-2 5-methyl-3-phenyl-oxazolidine 

Relevant articles and documents

Direct hydroxyethylation of amines by carbohydrates: Via ruthenium catalysis

An efficient and halogen-free catalytic methodology for the synthesis of β-amino alcohols from aromatic amines and biomass-derived carbohydrates is demonstrated for the first time. The activation of C5/C6 sugars by a ruthenium catalyst selectively generates the C2 alkylating reagent glycolaldehyde. The transformation involves metal-catalyzed hydrogen borrowing for the reduction of the imine intermediate. A series of arylamines bearing various substituents were successfully transformed into the desired products in good to excellent yields.

Mild and phosphine-free iron-catalyzed cross-coupling of nonactivated secondary alkyl halides with alkynyl grignard reagents

A simple protocol for iron-catalyzed cross-coupling of nonactivated secondary alkyl bromides and iodides with alkynyl Grignard reagents at room temperature has been developed. A wide range of secondary alkyl halides and terminal alkynes are tolerated to a

Process for preparing optically active secondary alcohols having nitrogenous or oxygenic functional groups

A process for preparing optically active secondary alcohols of the general formula (3), [wherein R1 is linear lower alkyl, an aromatic ring group, or the like; A is CH2NR2R3 or the like; n is an integer of 0 to 2; and * represents an asymmetric carbon atom] by asymmetrically hydrogenating a ketone compound of the general formula (1) having nitrogenous or oxygen functional group at any of the a-, β- and γ-positions, with selectivity among functional groups by the use of a ruthenium/optically active bidentate phosphine/diamine complex as the catalyst in the presence of hydrogen alone or together with a base. The optically active secondary alcohols obtained by the process are useful as drugs and intermediates for the preparation of drugs.