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32347-96-9

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32347-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32347-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,4 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32347-96:
(7*3)+(6*2)+(5*3)+(4*4)+(3*7)+(2*9)+(1*6)=109
109 % 10 = 9
So 32347-96-9 is a valid CAS Registry Number.

32347-96-9Relevant academic research and scientific papers

A convenient and efficient palladium-catalyzed system for cross-coupling of aryl bromides with active methylene compounds

Gao, Chengwei,Tao, Xiaochun,Qian, Yanlong,Huang, Jiling

, p. 1716 - 1718 (2003)

A simply catalytic system containing palladium-phosphine complex, generated in situ from PdCl2/tert-phosphino ligand in pyridine, has been systematically studied in the cross-coupling of bromobenzene with malononitrile or ethyl cyanoacetate anion. The effect of molar ratio of phosphine ligand to PdCl2 on the activity of the coupling was also discussed. It is found that the catalytic system has highly catalytic activity to produce aryl malononitriles and cyanoacetates in considerable yields (67-90%) when the substituted aryl bromides were used as substrates.

Preparation of O-Protected Cyanohydrins by Aerobic Oxidation of α-Substituted Malononitriles in the Presence of Diarylphosphine Oxides

Zhang, Dapeng,Lian, Mingming,Liu, Jia,Tang, Shukun,Liu, Guangzhi,Ma, Cunfei,Meng, Qingwei,Peng, Haisheng,Zhu, Daling

, p. 2597 - 2601 (2019/04/17)

A mild, reagent-cyanide-free, and efficient synthesis of O-phosphinoyl-protected cyanohydrins from readily available α-substituted malononitriles was realized using diarylphosphine oxides in the presence of O2. Mechanistic studies indicated that in addition to the initial aerobic oxidation of the malononitrile derivative notable features of this process include the formation of a tetrahedral intermediate and a subsequent intramolecular rearrangement. The phosphinoyl-protecting group can be removed by alcoholysis or by reduction with DIBAL-H.

Design and evaluation of pyrazolopyrimidines as KCNQ channel modulators

Osuma, Augustine T.,Xu, Xiangdong,Wang, Zhi,Van Camp, Jennifer A.,Freiberg, Gail M.

, (2019/08/13)

Effective treatments of neuropathic pain have been a focus of many discovery programs. KCNQ (kv7) are voltage gated potassium channel openers that have the potential for the treatment of CNS disorders including neuropathic pain. Clinical studies have sugg

Effect of Substituents on the Bond Strength of Air-Stable Dicyanomethyl Radical Thermochromes

Peterson, Joshua P.,Geraskina, Margarita R.,Zhang, Rui,Winter, Arthur H.

, p. 6497 - 6501 (2017/06/23)

A series of substituted aryl dicyanomethyl radicals were synthesized, and the bonding thermodynamic parameters for self-dimerization were determined from van't Hoff plots obtained from variable-temperature electron paramagnetic resonance and ultraviolet-v

A highly efficient catalytic system for cross-coupling of aryl chlorides and bromides with malononitrile anion by palladium carbene complexes

Gao, Chengwei,Tao, Xiaochun,Qian, Yanlong,Huang, Jiling

, p. 1444 - 1445 (2007/10/03)

Six imidazolium chlorides (1-6) as precursors of 1,3-diaryl substituted N-heterocyclic carbene ligands were synthesized and evaluated in palladium-catalyzed cross-coupling reactions of aryl chlorides and bromides with malononitrile in the presence of NaH.

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