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1821-39-2

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1821-39-2 Usage

General Description

Electropolymerization of 2-propylaniline in highly acidic medium yields poly(2-propylaniline) film. Polymerization and intercalation of 2-propylaniline into iron (III) oxychloride via in situ polymerization/intercalation process has been reported.

Check Digit Verification of cas no

The CAS Registry Mumber 1821-39-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1821-39:
(6*1)+(5*8)+(4*2)+(3*1)+(2*3)+(1*9)=72
72 % 10 = 2
So 1821-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N/c1-2-9(10)8-6-4-3-5-7-8/h3-7,9H,2,10H2,1H3

1821-39-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Propylaniline

1.2 Other means of identification

Product number -
Other names o-Aminopropylbenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1821-39-2 SDS

1821-39-2Relevant articles and documents

Synthesis of new sterically hindered anilines

Steele, Barry R.,Georgakopoulos, Spyros,Micha-Screttas, Maria,Screttas, Constantinos G.

, p. 3091 - 3094 (2007)

Ring-alkylated primary, secondary and tertiary anilines have been ethylated with ethylene at benzylic positions in a simple and inexpensive one-pot procedure which is mediated by the use of the superbase system nBuLi/LiK(OCH2CH2NMe2)2 in the presence of Mg(OCH2CH2OEt)2. Primary and secondary anilines are ethylated readily at ortho-benzylic positions but with difficulty or not at all at other positions. Tertiary anilines are ethylated at all positions. Mono- or diethylation occurs depending on the steric constraints present. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

Selective Synthesis of Primary Anilines from NH3 and Cyclohexanones by Utilizing Preferential Adsorption of Styrene on the Pd Nanoparticle Surface

Koizumi, Yu,Jin, Xiongjie,Yatabe, Takafumi,Miyazaki, Ray,Hasegawa, Jun-ya,Nozaki, Kyoko,Mizuno, Noritaka,Yamaguchi, Kazuya

supporting information, p. 10893 - 10897 (2019/07/12)

Dehydrogenative aromatization is one of the attractive alternative methods for directly synthesizing primary anilines from NH3 and cyclohexanones. However, the selective synthesis of primary anilines is quite difficult because the desired primary aniline products and the cyclohexanone substrates readily undergo condensation affording the corresponding imines (i.e., N-cyclohexylidene-anilines), followed by hydrogenation to produce N-cyclohexylanilines as the major products. In this study, primary anilines were selectively synthesized in the presence of supported Pd nanoparticle catalysts (e.g., Pd/HAP, HAP=hydroxyapatite, Ca10(PO4)6(OH)2) by utilizing competitive adsorption unique to heterogeneous catalysis; in other words, when styrene was used as a hydrogen acceptor, which preferentially adsorbs on the Pd nanoparticle surface in the presence of N-cyclohexylidene-anilines, various structurally diverse primary anilines were selectively synthesized from readily accessible NH3 and cyclohexanones. The Pd/HAP catalyst was reused several times though its catalytic performance gradually declined.

Simultaneous hydrodenitrogenation and hydrodesulfurization on unsupported Ni-Mo-W sulfides

Albersberger, Sylvia,Hein, Jennifer,Schreiber, Moritz W.,Guerra, Santiago,Han, Jinyi,Gutiérrez, Oliver Y.,Lercher, Johannes A.

, p. 344 - 355 (2017/09/30)

The catalytic properties of unsupported Ni-Mo-W sulfides (composites of Ni-Mo(W)S2 mixed sulfides and Ni3S2) obtained from precursors synthesized via co-precipitation, hydrothermal, and thiosalt decomposition were explored

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