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Propanedinitrile, [3-(4-methylphenyl)-3-oxo-1-phenylpropyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77609-10-0

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77609-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77609-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,0 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77609-10:
(7*7)+(6*7)+(5*6)+(4*0)+(3*9)+(2*1)+(1*0)=150
150 % 10 = 0
So 77609-10-0 is a valid CAS Registry Number.

77609-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-(4-methylphenyl)-3-oxo-1-phenylpropyl]propanedinitrile

1.2 Other means of identification

Product number -
Other names HMS1546A16

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:77609-10-0 SDS

77609-10-0Relevant academic research and scientific papers

Cu(II)-Promoted Cascade Synthesis of Fused Imidazo-Pyridine-Carbonitriles

Rakshit, Amitava,Dhara, Hirendra Nath,Alam, Tipu,Dahiya, Anjali,Patel, Bhisma K.

supporting information, p. 17504 - 17510 (2021/11/18)

A Cu(II)-promoted synthesis of an aza-fused N-heterocycle having a benz-imidazopyridine scaffold is developed via an addition-cyclization reaction followed by an Ullmann-type C-N coupling between o-iodoanilines and γ-ketodinitriles. This protocol features a broad substrate scope, giving products in 32-84% yields. The compounds show excellent photoluminescence properties having two absorption maxima in the region between 270-280 and 338-350 nm and emission maxima in the range of 502-533 nm. The HOMO-LUMO energy gap of 3.49-3.57 eV was determined using Gaussian 09 at the B3LYP/6-31G (d, p) basis set level. We also demonstrated a few postsynthetic modifications.

Visible-light-accelerated pd-catalyzed cascade addition/ cyclization of arylboronic acids to γ- And β-ketodinitriles for the construction of 3-cyanopyridines and 3-cyanopyrrole analogues

Patel, Bhisma K.,Rakshit, Amitava,Kumar, Prashant,Alam, Tipu,Dhara, Hirendranath

, p. 12482 - 12504 (2020/11/09)

The one-pot synthetic strategies for 2,4,6-triarylnicotinonitriles and 2,5-diaryl-1H-pyrrole-3-carbonitriles have been accomplished via a Pd-catalyzed coupling of arylboronic acid with 2-(3-oxo-1,3-diarylpropyl)malononitrile and 2-(2-oxo-2- arylethyl)malo

Immobilization of lipase on Fe3O4/ZnO core/shell magnetic nanoparticles and catalysis of Michael-type addition to chalcone derivatives

Ghasemi, Sabrieh,Heidary, Marjan,Faramarzi, Mohammad Ali,Habibi, Zohreh

, p. 121 - 128 (2014/01/23)

Fe3O4/ZnO core/shell magnetic nanoparticles in 1:1 and 1:2 molar ratios were prepared and characterized by using X-ray powder diffraction, scanning electron microscopy, thermogravimetric analysis, FT-IR spectra, and flame atomic abso

A mild and convenient one-pot synthesis of 4,6-diaryl- 3-aminoisoxazolo[3, 4-b]pyridines

Miao, Chun-Bao,Wang, Yan-Hong,Dong, Chun-Ping,Yang, Hai-Tao,Meng, Qi,Sun, Xiao-Qiang

, p. 2599 - 2605 (2014/01/06)

We have developed a convenient method for the synthesis of a series of new 4,6-diaryl-3-aminoisoxazolo[3,4-b]pyridines through one-pot reaction starting from the easily available chalcones, malononitrile, and hydroxylamine. This class of compounds might h

A convenient synthesis of (3-oxo-1,3-diaryl) propylpropanedinitrile catalyzed by KF-alumina

Shi,Lu,Wang,Tu,Dai

, p. 4003 - 4007 (2007/10/03)

A series of (3-oxo-1,3-diaryl) propylpropanedinitriles were synthesized by Michael addition reaction of chalcones and malononitriles in the presence of potassium fluoride on alumina.

SYNTHESIS AND SOME REACTIONS OF 3-CYANOPYRIDINE-2-THIONES

Krauze, A. A.,Bomika, Z. A.,Shestopalov, A. M.,Rodinovskaya, L. A.,Pelcher, Yu. E',et al.

, p. 279 - 284 (2007/10/02)

New method for the synthesis of 3-cyanopyridine-2-thiones by the reaction of δ-keto nitroles with sulfur and by condensation of chalcones or benzylideneacetone with cyanothioacetamide are given.The compounds obtained were used in various reactions for the preparation of alkylated products, disulfides, and condensed heterocycles, viz., thienopyridines and pyridothienopyrimidines.

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