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N1,N2-diphenyl-N3-diisopropoxyphosphinoylguanidine is a complex organic compound with the molecular formula C21H26N5O2P. It is a derivative of guanidine, featuring two phenyl groups attached to the N1 and N2 positions, and a diisopropoxyphosphinoyl group at the N3 position. N1,N2-diphenyl-N3-diisopropoxyphosphinoylguanidine is known for its potential applications in the field of agrochemicals, particularly as a herbicide. It works by inhibiting the enzyme acetohydroxyacid synthase, which is crucial for the synthesis of branched-chain amino acids in plants, thus affecting their growth. The diisopropoxyphosphinoyl group contributes to the compound's herbicidal activity, while the phenyl groups may influence its chemical stability and biological activity. Due to its specific mode of action and structure, it is an important compound in the development of new herbicides that can target resistant weeds in agriculture.

6682-95-7

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6682-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6682-95-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,8 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6682-95:
(6*6)+(5*6)+(4*8)+(3*2)+(2*9)+(1*5)=127
127 % 10 = 7
So 6682-95-7 is a valid CAS Registry Number.

6682-95-7Downstream Products

6682-95-7Relevant academic research and scientific papers

SOME TRANSFORMATIONS OF N-(THIO)PHOSPHORYLATED S-ALKYL AND S-ACYLISOTHIOUREAS. SYNTHESIS AND PROPERTIES OF PHOSPHORYLATED CARBODIIMIDES

Kamalov, R. M.,Khailova, N. A.,Pudovik, M. A.

, p. 837 - 841 (2007/10/02)

In the course of vacuum fractionation, N-(thio)phosphoryl-S-allylisothioureas are converted to N-(thio)phosphorylcarbodiimides.These latter were also obtained by elimination of H2S from N-(thio)phosphorylureas under conditions of Appel reaction or by reaction of (thio)phosphoric isothiocyanates with phosphinimine (Staudinger reaction), the latter method giving better results.Reactions of N-thiophosphorylthioureas with acetyl chloride or phenyl isothiocyanate yield mostly thiophosphorylated isothiocyanates, while reactions with chloroformamidine yield both isothiocyanates and carbodiimides.A synthesis is reported of 2-thiophosphoryliminoimidazolidines by reaction of thiophosphorylcarbodiimides with 2-bromoethylammonium bromide.

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