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961-38-6

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961-38-6 Usage

Chemical Properties

White to off-white powder

Uses

Different sources of media describe the Uses of 961-38-6 differently. You can refer to the following data:
1. 2,4,6-Tri-tert-butylnitrobenzene (bulky amine) is used in the synthesis of monomeric iminophosphorane
2. 2,4,6-Tri-tert-butylnitrobenzene (bulky amine) was used in the synthesis of monomeric iminophosphorane.

Check Digit Verification of cas no

The CAS Registry Mumber 961-38-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 961-38:
(5*9)+(4*6)+(3*1)+(2*3)+(1*8)=86
86 % 10 = 6
So 961-38-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H31N/c1-16(2,3)12-10-13(17(4,5)6)15(19)14(11-12)18(7,8)9/h10-11H,19H2,1-9H3

961-38-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (L01362)  2,4,6-Tri-tert-butylaniline, 95%   

  • 961-38-6

  • 1g

  • 428.0CNY

  • Detail
  • Alfa Aesar

  • (L01362)  2,4,6-Tri-tert-butylaniline, 95%   

  • 961-38-6

  • 5g

  • 1002.0CNY

  • Detail

961-38-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-Tri-Tert-Butylaniline

1.2 Other means of identification

Product number -
Other names 2,4,6-tritert-butylaniline

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:961-38-6 SDS

961-38-6Relevant articles and documents

Ultrasmall and Stable Pd and Pt Nanoparticles Within Zeolite HY Through Impregnated Method with Enhanced Semihydrogenation Selectivity

Wang, Mengyue,Liu, Xuan,Ren, Kui,Zhou, Yiming,Li, Tianhao,Bi, Yunfei,Kang, Haozhe,Xing, Enhui,Chen, Qiang

, p. 2684 - 2695 (2021/01/13)

In this study, with zeolite HY as support, ultrasmall Pd and Pt nanoparticles were successfully immobilized into zeolite HY crystals through an optimized impregnation approach. The success of this new approach mainly relied on the selecting appropriate metal precursor to make Pd and Pt element exists with the cation forms, which can facilitate their diffusion into inner channels of zeolite HY through electrostatic attraction and capillary force. Integration of confinement effect of zeolite HY, taking zeolite HY (Si/Al = 3) encapsulation of ultrasmall Pd NPs (Pd@HY-3) as an instance, Pd@HY-3 catalyst exhibited enhanced catalytic selectivity in semihydrogenation of alkynes, in comparison with Pd/HY, Pd/C, Pd/Al2O3 and lindlar catalysts. This improved catalytic selectivity can be attributed to the constrained upright adsorption conformation of reactant alkyne and corresponding product alkene on encapsulated Pd surface to make alkyne adsorption on Pd surface with larger adsorption energy than that of alkene, thus achieving the high catalytic selectivity. Graphic Abstract: [Figure not available: see fulltext.]

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

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Page/Page column 31-32, (2018/07/29)

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.

Biomass-Derived Catalysts for Selective Hydrogenation of Nitroarenes

Sahoo, Basudev,Formenti, Dario,Topf, Christoph,Bachmann, Stephan,Scalone, Michelangelo,Junge, Kathrin,Beller, Matthias

, p. 3035 - 3039 (2017/08/18)

Development of catalytically active materials from biowaste represents an important aspect of sustainable chemical research. Three heterogeneous materials were synthesized from inexpensive biomass-based chitosan and abundant Co(OAc)2 using complexation followed by pyrolysis at various temperatures. These materials were applied in the catalytic hydrogenation of nitroarenes using molecular hydrogen. A variety of diversely functionalized nitroarenes including some pharmaceutically active compounds were converted into aromatic amines in high yields, with high selectivity, and with excellent functional group tolerance. This green protocol has also been implemented for the synthesis of a biologically important TRPC3 inhibitor.

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