268887
2-Isopropylaniline
97%
Synonym(s):
o-Aminocumene
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About This Item
Linear Formula:
(CH3)2CHC6H4NH2
CAS Number:
Molecular Weight:
135.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-397-7
Beilstein/REAXYS Number:
636283
MDL number:
Assay:
97%
Form:
liquid
InChI key
YKOLZVXSPGIIBJ-UHFFFAOYSA-N
InChI
1S/C9H13N/c1-7(2)8-5-3-4-6-9(8)10/h3-7H,10H2,1-2H3
SMILES string
CC(C)c1ccccc1N
vapor pressure
0.05 mmHg ( 20 °C)
assay
97%
form
liquid
Quality Level
bp
112-113 °C/18 mmHg (lit.)
density
0.955 g/mL at 25 °C (lit.)
Related Categories
General description
The reactions of 1,1′-bis(hydroxymethyl)ferrocene with 2-isopropylaniline, in the presence of a catalyst [RuCl2(PPh3)3], was studied.
Application
2-Isopropylaniline was used in the synthesis of a colorless amine-coordinated zinc complex.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
204.8 °F - closed cup
flash_point_c
96 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Dongzhen Li et al.
Organic & biomolecular chemistry, 8(8), 1816-1820 (2010-05-08)
Zn(OTf)(2) acts as an excellent catalyst precursor for addition of various amine N-H bonds to carbodiimides under an atmosphere of air, offering a convenient synthesis of substituted guanidines with high functional-group tolerance. A Zn-N amido species is shown to act
Further Investigation on Preparation, Structure and Electrochemical Properties of N-Alkyl-and N-Aryl-2-aza-[3]-ferrocenophanes.
Sakano T, et al.
Bulletin of the Chemical Society of Japan, 74(11), 2059-2065 (2001)
Junbin Ji et al.
Applied microbiology and biotechnology, 103(15), 6333-6344 (2019-05-24)
The residues of aniline and its derivatives are serious environment pollutants. Aniline dioxygenase (AD) derived from aerobic bacteria catalyzes the conversion of aniline to catechol, which has potential use in the bioremediation of aromatic amines and biorefining process. AD contains
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