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

77609-07-5

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77609-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77609-07-5 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, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77609-07:
(7*7)+(6*7)+(5*6)+(4*0)+(3*9)+(2*0)+(1*7)=155
155 % 10 = 5
So 77609-07-5 is a valid CAS Registry Number.

77609-07-5SDS

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

1.2 Other means of identification

Product number -
Other names -

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:77609-07-5 SDS

77609-07-5Relevant articles and documents

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

One-Pot Quinine-Catalyzed Synthesis of α-Chiral γ-Keto Esters: Enantioenriched Precursors of cis-α,γ-Substituted-γ-Butyrolactones

Meninno, Sara,Volpe, Chiara,Lattanzi, Alessandra

supporting information, p. 2845 - 2848 (2016/09/13)

A highly enantioselective one-pot synthesis of important building blocks, α-chiral γ-keto esters, has been developed by combining a quinine-catalyzed Michael addition of malononitrile to trans-enones followed by magnesium monoperoxyphthalate (MMPP) oxidat

Conjugate addition of malononitrile on chalcone: Biocatalytic [Formula presented] bond formation

Punyapreddiwar, Nitesh D.,Zodape, Sangesh P.,Wankhade, Atul V.,Pratap, Umesh R.

, p. 124 - 126 (2016/08/23)

An efficient, cost effective and environmentally friendly protocol has been developed for the Michael addition of malononitrile on 1,3-diaryl-2-propen-1-ones (Chalcones) using very cheaper, easily available natural catalyst, baker's yeast. The whole cells of yeast excellently worked in nonaqueous medium, ethanol without decrease in catalytic activity.

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

An active and selective heterogeneous catalytic system for Michael addition

Keipour, Hoda,Khalilzadeh, Mohammad A.,Hosseini, Abolfazl,Pilevar, Afsaneh,Zareyee, Daryoush

experimental part, p. 537 - 540 (2012/06/29)

Potassium fluoride doped natural zeolite was found to be an efficient and selective solid base catalyst for 1,4-Michael addition. The catalyst is easily prepared and the workup procedure simplified by simple filtration. All products were obtained in high

The Michael addition of active methylene compounds to chalcone derivatives using a catalytic amount of iodine and K2CO3 at room temperature

Ren, Yi-Ming,Cai, Chun

experimental part, p. 176 - 178 (2011/07/31)

A convenient method for the Michael addition of active methylene compounds to chalcone derivatives has been developed using the inexpensive and environmentally friendly reagent I2/K2CO3 at room temperature. The method is m

A facile and efficient one-pot synthesis of polysubstituted benzenes in guanidinium ionic liquids

Xin, Xin,Wang, Yan,Xu, Wu,Lin, Yingjie,Duan, Haifeng,Dong, Dewen

body text, p. 893 - 898 (2010/09/05)

A facile and efficient synthesis of polysubstituted benzenes has been developed via sequential Michael addition, Knoevenagel condensation and nucleophilic cyclization reactions of readily available chalcones with active methylene compounds in guanidinium

Back to natural cinchona alkaloids: Highly enantioselective Michael addition of malononitrile to enones

Russo, Alessio,Perfetto, Alessandra,Lattanzi, Alessandra

supporting information; experimental part, p. 3067 - 3071 (2010/04/06)

An efficient and convenient highly enantioselective Michael addition of malononitrile to enones has been developed by using quinine as the organocatalyst. The adducts were isolated in excellent yield and high asymmetric induction (up to 95% ee). An easy r

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