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Benzamide, N,N'-[1,2-ethanediylbis(iminocarbonothioyl)]bis-, also known as bis(N-benzoylthiocarbamoyl)ethane or N,N'-ethylenebis(N-benzoylthiocarbamate), is a chemical compound with the molecular formula C18H16N2O2S2. It is a white crystalline solid that is soluble in organic solvents. Benzamide, N,N'-[1,2-ethanediylbis(iminocarbonothioyl)]bis- is primarily used as a pesticide, specifically as a herbicide, to control the growth of unwanted plants in agricultural settings. It works by inhibiting the enzyme acetohydroxyacid synthase, which is essential for plant growth. The chemical structure of Benzamide, N,N'-[1,2-ethanediylbis(iminocarbonothioyl)]bis- features two benzamide groups connected by a central ethylene bridge, with each benzamide group further linked to a thiocarbonyl group.

7710-08-9

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7710-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7710-08-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7710-08:
(6*7)+(5*7)+(4*1)+(3*0)+(2*0)+(1*8)=89
89 % 10 = 9
So 7710-08-9 is a valid CAS Registry Number.

7710-08-9Downstream Products

7710-08-9Relevant academic research and scientific papers

Synthesis and antibacterial activity of copper(I) complexes with bisbenzoylthiourea

Zhao, Meng-Meng,Dong, Xiu-Yan,Li, Gang,Yang, Xiao-Qin

, p. 277 - 279 (2014)

Two copper(I) complexes, [Cu(L)]ClO4 (1) and [Cu(L)Cl]?C2H5OH (2), have been synthesized by the reaction of copper(II) perchlorate hexahydrate and copper(II) chloride dihydrate with N,N'-(1,2-dimethylene)bisbenzoylthiourea (L), respectively and characteri

Synthesis, characterization and biological activity of some dithiourea derivatives

Frost, Carminita,Hoppe, Heinrich,Hosten, Eric,Isaacs, Michelle,Khanye, Setshaba D.,Krause, Jason,Lobb, Kevin,Odame, Felix,Sayed, Yasien,Tshentu, Zenixole

, p. 764 - 777 (2020/10/02)

Novel dithiourea derivatives have been designed as HIV-1 protease inhibitors using Autodock 4.2, synthesized and characterized by spectroscopic methods and microanalysis. 1-(3-Bromobenzoyl)-3-[2-({[(3-bromophenyl)formami-do]methanethioyl}amino)phenyl]thio

Dihydrogen phosphate-containing dinuclear double assemblies that demonstrate phosphate reactivity to the tetrafluoroborate anion

Faulkner, Robert A.,Patmore, Nathan J.,Rice, Craig R.,Slater, Christopher

supporting information, p. 9159 - 9162 (2018/08/23)

The ligands L1 and L2 both form dinuclear assemblies with Cu(ii) and these react with dihydrogen phosphate so that the anion is incorporated within the assembly (e.g. [Cu2L2(H2PO4)]3+). However, in the presence of tetrafluoroborate anions the phosphate undergoes reaction with the anion forming [Cu3(L1)3(O3POBF3)]3+ and [Cu2(L2)2(O2P(OBF3)2)]+.

Antituberculosis and antifungal activities of synthesized benzoylthiourea derivatives

Zhao, Meng-Meng,Dong, Xiu-Yan,Li, Gang,Yang, Yu-Hua,Zhang, Yu-Jie,Yang, Xiao-Qin

, p. 7551 - 7553 (2013/08/23)

A series of benzoylthiourea derivatives have been synthesized from benzoyl isothiocyanate and phenyleneamine in CH2Cl2 medium under solid-liquid phase transfer catalysis conditions. Structures of these compounds have been characteriz

An efficient synthesis of polymethylene-bis-aroyl thiourea derivatives under the condition of phase-transfer catalysis

Zhang, You-Ming,Wei, Tai-Bao,Xian, Liang,Gao, Li-Ming

, p. 2007 - 2013 (2007/10/03)

Reaction of polymethylene diamine with aroyl chloride and ammonium thiocyanate under the condition of solid-liquid phase-transfer catalysis using polyethylene glycol-400 (PEG-400) as the catalyst yielded polymethylene-bis- aroyl thiourea derivatives 3a-q

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