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4'-(N,N-dimethylamino)-2-nitrodiphenylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129880-96-2

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129880-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129880-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,8 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129880-96:
(8*1)+(7*2)+(6*9)+(5*8)+(4*8)+(3*0)+(2*9)+(1*6)=172
172 % 10 = 2
So 129880-96-2 is a valid CAS Registry Number.

129880-96-2Relevant academic research and scientific papers

Inter- And intramolecular photoinduced electron transfer of flavin derivatives with extremely small reorganization energies

Murakami, Motonobu,Ohkubo, Kei,Fukuzumi, Shunichi

, p. 7820 - 7832 (2010)

Photoinduced electron transfer (ET) of a series of aromatic electron donors (D) to the singlet or triplet excited state of a flavin analogue (10methylisoalloxazine: MeFl) and intermolecular back electron transfer (BET) from MeFl to D+ in benzon

A versatile method for the synthesis of benzimidazoles from o-nitroanilines and aldehydes in one step via a reductive cyclization

Yang, Donglai,Fokas, Demosthenes,Li, Jingzhou,Yu, Libing,Baldino, Carmen M.

, p. 47 - 56 (2007/10/03)

A highly efficient and versatile method for the synthesis of benzimidazoles was achieved in one step via the Na2S2O4 reduction of o-nitroanilines in the presence of aldehydes. Heating a solution of o-nitroaniline (Ic) and an aldehyde in EtOH or another appropriate solvent, in the presence of aqueous or solid Na2S2O4, provided facile access to a series of 2-substituted N-H benzimidazoles 5a-m containing a wide range of functional groups not always compatible with the existing synthetic methods. This methodology has also been applied to the regioselective synthesis of N-alkyl and N-aryl benzimidazoles 6a-f via the cyclization of the corresponding N-substituted nitroanilines 13a-e, respectively. In addition, the method was applied successfully to the synthesis of other imidazole containing heterocyclic ring systems such as 1H-imidazo[4,5-b]pyridines 14a,b and 1H-imidazo[4,5-f]quinoline 15.

Flavins as potential antimalarials. 2. 3-Methyl-10-(substituted-phenyl)flavins

Cowden,Halladay,Cunningham,Hunt,Clark

, p. 1818 - 1822 (2007/10/02)

A series of 3-methyl-10-(substituted-phenyl)flavins was prepared and tested for antimalarial activity against the lethal parasite Plasmodium vinckei in mice. Several of these analogues were found to be effective antimalarial agents. A quantitative structure-activity relationship study was undertaken with 44 analogues and no satisfactory relationship could be established.

New Modified Preparation of 2-Nitrodiarylamines

Zhu, Yun-Fei,Lin, Guo-Qiang,Chen, Yu-Qun

, p. 430 (2007/10/02)

2-Nitrodiarylamines are prepared in good yields from 2-chloronitrobenzene and anilines in the presence of potassium fluoride without solvent at 160-170 deg C.

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