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3-(TERT-BUTYLAMINO)PROPIONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21539-53-7

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21539-53-7 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 81, p. 5333, 1959 DOI: 10.1021/ja01529a023

Check Digit Verification of cas no

The CAS Registry Mumber 21539-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,3 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21539-53:
(7*2)+(6*1)+(5*5)+(4*3)+(3*9)+(2*5)+(1*3)=97
97 % 10 = 7
So 21539-53-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2/c1-7(2,3)9-6-4-5-8/h9H,4,6H2,1-3H3

21539-53-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(tert-Butylamino)propionitrile

1.2 Other means of identification

Product number -
Other names 3-(tert-butylamino)propanenitrile

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:21539-53-7 SDS

21539-53-7Relevant academic research and scientific papers

Palladium nanoparticles in glycerol: A versatile catalytic system for C-X bond formation and hydrogenation processes

Chahdoura, Faouzi,Pradel, Christian,Gomez, Montserrat

supporting information, p. 3648 - 3660 (2014/01/06)

Palladium nanoparticles stabilised by tris(3-sulfophenyl)phosphine trisodium salt in neat glycerol have been synthesised and fully characterised, starting from both Pd(II) and Pd(0) species. The versatility of this innovative catalytic colloidal solution has been proved by its efficient application in C-X bond formation processes (X=C, N, P, S) and C-C multiple bond hydrogenation reactions. The catalytic glycerol phase could be recycled more than ten times, preserving its activity and selectivity. The scope of each of these processes has demonstrated the power of the as-prepared catalyst, isolating the corresponding expected products in yields higher than 90%. The dual catalytic behaviour of this glycerol phase, associated to the metallic nanocatalysts used in wet medium (molecular- and surface-like behaviour), has allowed attractive applications in one-pot multi-step transformations catalysed by palladium, such as C-C coupling followed by hydrogenation, without isolation of intermediates using only one catalytic precursor. Copyright

Solid sodium stannate as a high-efficiency superbase catalyst for anti-Markovnikov hydroamination and hydroalkoxylation of electron-deficient olefins under mild conditions

Zhang, Shuguo,Wei, Yudan,Yin, Shuangfeng,Au, Chak-Tong

, p. 712 - 716 (2013/01/09)

A solid superbase with H- above 26.5 has been obtained through thermal treatment of sodium stannate hydrate. It was found to be an efficient catalyst for anti-Markovnikov hydroamination and hydroalkoxylation of electron-deficient olefins under mild conditions.

Synthesis of substituted aziridines via intramolecular reactions of β-N-chloroethylamino carbanions

Makosza, Mieczyslaw,Bobryk, Karolina,Krajewski, Dariusz

experimental part, p. 1511 - 1524 (2009/07/17)

Simple and efficient method of synthesis of 2-alkoxycarbonyl, 2-cyano, 2-phenylsulfonyl N-alkylaziridines was elaborated via intramolecular nucleophiles substitution of chloride in 1-N-chloro-2-alkoxycarbonyl (cyano, phenylsulfonyl) ethyl amines. These su

High-pressure effect on organic reactions in fluorophobic media

Jenner, Gerard,Gacem, Badra

, p. 265 - 270 (2007/10/03)

The kinetic effect of fluorophobic interactions was examined in Diels-Alder reactions and the conjugate addition of amines to acrylonitrile at different pressures. Its magnitude is lower than for other solvophobic media (water, ethylene glycol). Activatio

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