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15190-06-4

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15190-06-4 Usage

Description

(2R)-[(4-methylphenyl)amino](phenyl)ethanenitrile is a chiral molecule with a molecular formula of C15H14N2. It is composed of a phenyl group, a 4-methylphenyl group, an amino group, and a nitrile group attached to a chiral carbon center. This unique structure and its chiral nature make it valuable for creating diverse chemical structures and studying their potential biological activities.

Uses

Used in Organic Synthesis:
(2R)-[(4-methylphenyl)amino](phenyl)ethanenitrile is used as a building block in organic synthesis for the production of various drugs and biologically active molecules. Its unique structure allows for the creation of diverse chemical structures, making it a valuable component in the synthesis of complex organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2R)-[(4-methylphenyl)amino](phenyl)ethanenitrile is used as a key intermediate in the development of new drugs and biologically active molecules. Its chiral nature enables researchers to explore the effects of different stereoisomers on biological activity, potentially leading to the discovery of more effective and selective medications.

Check Digit Verification of cas no

The CAS Registry Mumber 15190-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,9 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15190-06:
(7*1)+(6*5)+(5*1)+(4*9)+(3*0)+(2*0)+(1*6)=84
84 % 10 = 4
So 15190-06-4 is a valid CAS Registry Number.

15190-06-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-(4-methylanilino)-2-phenylacetonitrile

1.2 Other means of identification

Product number -
Other names methylphenylthiazolane

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:15190-06-4 SDS

15190-06-4Relevant articles and documents

A unique combination of KI/ZnFe2O4 as a catalyst for oxidative Strecker reaction

Ghandi, Leila,Kazemi Miraki, Maryam,Karimi, Meghdad,Radfar, Iman,Heydari, Akbar

, (2019)

α-Aminonitriles as key intermediates for the preparation of α-amino acid derivatives, amides, diamines, peptides, proteins and heterocycles were synthesized through methylarene oxidation in the Strecker reaction using a unique combination of KI/ZnFe2O4 as the best catalyst and aqueous tert-butyl hydroperoxide as oxidant. A wide range of amines and methylarenes were converted to the corresponding products. Operational simplicity, short reaction time and recyclability of the catalyst are advantages of this protocol.

A Metal-Organic Framework to CuO Nanospheres of Uniform Morphology for the Synthesis of α-Aminonitriles under Solvent-Free Condition along with Crystal Structure of the Framework

Singha, Soumen,Saha, Arijit,Goswami, Somen,Dey, Sanjoy Kumar,Payra, Soumen,Banerjee, Subhash,Kumar, Sanjay,Saha, Rajat

, p. 189 - 199 (2018)

Herein, we have reported the synthesis, crystal structure, thermogravimetric property, and photoluminescence activity of a new Cu-based metal organic framework (MOF): {[Cu2(2,5-pdc)2(ald-4)(H2O)2]·3H2

Targeted development of hydrophilic porous polysulfonamide gels with catalytic activity

Alavinia, Sedigheh,Ghorbani-Vaghei, Ramin

, (2020/07/03)

We report the use of a template and functional monomers in the synthesis of three novel polysulfonamide gels with new architectures and functional groups. These mesoporous polysulfonamide gels were prepared by the condensation polymerization of benzene-1,3-disulfonyl chloride (as the main precursor), linear monomers, and cross-linkers (as variable precursors) in the presence of a silica template by a combination of sol-gel chemistry and the nanocasting technique. In this synthesis pathway, in situ polymerization onto the template surface led to the construction of a silica/polymer nanocomposite. Next, after removal of the template, the nanocomposite gels were transformed into mesoporous polysulfonamide nanospheres. After the physicochemical identification of the synthesized materials, functionalized polysulfonamides were used as reusable novel catalysts with high efficiency for the Strecker reaction under mild conditions. These polymers have Br?nsted/Lewis acid active sites, a mesoporous structure, and hydrogen bonding. Moreover, since these polymers are hydrogels that can absorb water, they can promote the Strecker reaction through chemical absorption of the generated water as a driving force. Overall, this article describes a novel synthesis procedure and application of porous polysulfonamide gels.

Strecker reactions with hexacyanoferrates as non-toxic cyanide sources

Grundke, Caroline,Opatz, Till

supporting information, p. 2362 - 2366 (2019/05/17)

The Strecker reaction is the most widely applied three-component reaction. Although highly useful for the preparation of α-amino nitriles, α-amino acids, hydantoins and numerous related compounds, the need for the application of toxic sources of HCN limits its application in both academic and industrial settings. Here, we present a facile protocol for Strecker reactions using a mixture of potassium ferri- and ferrocyanides as a non-toxic substitute.

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