643-28-7

Basic information

• Product Name: 2-ISOPROPYLANILINE
• Synonyms: O-ISOPROPYLANILINE;O-CUMIDINE;O-AMINOCUMENE;1-Amino-2-isopropylbenzene;2-Isopropylaniline, 97% 5ML;2-Aminocumene o-Cumidine;(2-Isopropylphenyl)amine;2-(Prop-2-yl)aniline, 2-Aminocumene
• CAS NO: 643-28-7
• Molecular Formula: C₉H₁₃N
• Molecular Weight: 135.21
• EINECS: 211-397-7
• Product Categories: Anilines, Aromatic Amines and Nitro Compounds
• Mol File: 643-28-7.mol
• Article Data: 35

Chemical Properties

• Melting Point: -6.87°C (estimate)
• Boiling Point: 112-113 °C18 mm Hg(lit.)
• Flash Point: 204 °F
• Appearance: Clear pale yellow to orange or brown/Liquid
• Density: 0.955 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.05 mm Hg ( 20 °C)
• Refractive Index: n20/D 1.548(lit.)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 4.42±0.10(Predicted)
• Water Solubility: Insoluble in water.
• Sensitive: Light Sensitive
• BRN: 636283
• CAS DataBase Reference: 2-ISOPROPYLANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ISOPROPYLANILINE(643-28-7)
• EPA Substance Registry System: 2-ISOPROPYLANILINE(643-28-7)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26-37/39
• WGK Germany: 3
• RTECS: BY4200000
• TSCA: Yes
• Hazardous Substances Data: 643-28-7(Hazardous Substances Data)

Usage

Chemical Properties

Clear pale yellow liquid

Uses

Different sources of media describe the Uses of 643-28-7 differently. You can refer to the following data:
1. Reagent in determination of tungsten.
2. 2-Isopropylaniline is used in the synthesis of a colorless amine-coordinated zinc complex. The reactions of 1,1?-bis(hydroxymethyl)ferrocene with 2-isopropylaniline, in the presence of a catalyst [RuCl2(PPh3)3], was studied

General Description

The reactions of 1,1′-bis(hydroxymethyl)ferrocene with 2-isopropylaniline, in the presence of a catalyst [RuCl2(PPh3)3], was studied.

InChI:InChI=1/C9H13N/c1-7(2)8-5-3-4-6-9(8)10/h3-7H,10H2,1-2H3

Upstream product

• 98-82-8 Isopropylbenzene 
• 67-56-1 methanol 
• 6526-72-3 o-nitrocumene 
• 201230-82-2 carbon monoxide 
• 7647-01-0 hydrogenchloride 
• 75-07-0 acetaldehyde 
• 78-84-2 isobutyraldehyde 
• 62-53-3 aniline 
• 859174-95-1 3-amino-4-isopropylbenzoic acid 
• 7073-94-1 1-bromo-2-isopropylbenzene 
• 88-69-7 2-(1-methylethyl)phenol 
• 7117-18-2 2-isopropyl-N-methylaniline 
• 406720-50-1 tert-butyl N-(2-isopropylphenyl)carbamate 
• 1616246-59-3 1-(4-methoxybenzyl)-3-methyl-1H-indole 

Downstream Products

• 19246-04-9 N-(2-isopropylphenyl)acetamide 
• 93007-80-8 2-benzamido-1-isopropylbenzene 
• 101287-23-4 N-(2-isopropylphenyl)-4-methylbenzenesulfonamide 
• 90874-73-0 N-(2-isopropylphenyl)formamide 
• 62655-20-3 1,3-dibromo-5-isopropylbenzene 
• 120-72-9 indole 
• 88-69-7 2-(1-methylethyl)phenol 
• 19099-54-8 2-isopropyliodobenzene 
• 117146-34-6 2-(2-isopropylphenylthio)acetic acid 
• 1627-75-4 3-methyl-isoxazole-4,5-dione 4-[(2-isopropyl-phenyl)-hydrazone] 
• 35452-49-4 N-benzyl-2-isopropylaniline 
• 97053-12-8 1-(2-Isopropyl-phenyl)-piperidine 
• 107379-93-1 (2-Isopropyl-phenyl)-[1-(4-nitro-phenyl)-meth-(E)-ylidene]-amine 
• 25343-23-1 N-((2-isopropylphenyl)carbamothioyl)benzamide 

Relevant articles and documents

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Mild deprotection of the: N-tert -butyloxycarbonyl (N -Boc) group using oxalyl chloride

We report a mild method for the selective deprotection of the N-Boc group from a structurally diverse set of compounds, encompassing aliphatic, aromatic, and heterocyclic substrates by using oxalyl chloride in methanol. The reactions take place under room temperature conditions for 1-4 h with yields up to 90percent. This mild procedure was applied to a hybrid, medicinally active compound FC1, which is a novel dual inhibitor of IDO1 and DNA Pol gamma. A broader mechanism involving the electrophilic character of oxalyl chloride is postulated for this deprotection strategy. This journal is

NITROGEN-CONTAINING BIOPOLYMER-BASED CATALYSTS, THEIR PREPARATION AND USES IN HYDROGENATION PROCESSES, REDUCTIVE DEHALOGENATION AND OXIDATION

The present invention relates to a process for the preparation of a nitrogen containing biopolymer-based catalyst by pyrolysis of a metal complex with a nitrogen-containing biopolymer and to the nitrogen containing biopolymer-based catalysts obtainable by this process. In particular, the invention relates to a nitrogen containing biopolymer-based catalyst comprising metal particles and at least one nitrogen containing carbon layer. The invention also relates to the use of a nitrogen containing biopolymer-based catalyst in a hydrogenation process, preferably in a process for hydrogenation of nitroarenes, nitriles or imines; in a reductive dehalogenation process of C-X bonds, wherein X is CI, Br or I, preferably in a process for dehalogenation of organohalides or in a process for deuterium labelling of arenes via dehalogenation of organohalides; or in an oxidation process. Further, the invention relates to a metal complex with the nitrogen containing biopolymer, wherein the metal is a transition metal selected from the group consisting of manganese, ruthenium, cobalt, rhodium, nickel, palladium and platinum, preferably cobalt or nickel, and wherein the nitrogen containing biopolymer is selected from chitosan, chitin and a polyamino acid, preferably chitosan or chitin.