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268887

Sigma-Aldrich

2-Isopropylaniline

97%

Synonym(s):

o-Aminocumene

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About This Item

Linear Formula:
(CH3)2CHC6H4NH2
CAS Number:
643-28-7
Molecular Weight:
135.21
Beilstein/REAXYS Number:
636283
EC Number:
211-397-7
MDL number:
MFCD00007720
UNSPSC Code:
12352100
PubChem Substance ID:
24856299
NACRES:
NA.22

vapor pressure

0.05 mmHg ( 20 °C)

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.548 (lit.)

bp

112-113 °C/18 mmHg (lit.)

density

0.955 g/mL at 25 °C (lit.)

SMILES string

CC(C)c1ccccc1N

InChI

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

InChI key

YKOLZVXSPGIIBJ-UHFFFAOYSA-N

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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.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk_germany

WGK 3

flash_point_f

204.8 °F

flash_point_c

96 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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.
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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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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

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