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Trimethyl N-(2-tolyl)-phosphorimidate is an organophosphorus compound with the chemical formula C10H15NPO. It is a colorless liquid that is soluble in organic solvents. trimethyl N-(2-tolyl)-phosphorimidate is primarily used as a reagent in organic synthesis, particularly in the formation of phosphorus-containing compounds. It is also known for its potential applications in the synthesis of pesticides and pharmaceuticals. The compound is characterized by its ability to react with various functional groups, making it a versatile tool in the field of chemistry. It is important to handle this chemical with care due to its potential toxicity and reactivity.

25615-91-2

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25615-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25615-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,1 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25615-91:
(7*2)+(6*5)+(5*6)+(4*1)+(3*5)+(2*9)+(1*1)=112
112 % 10 = 2
So 25615-91-2 is a valid CAS Registry Number.

25615-91-2Relevant academic research and scientific papers

The Chemistry of Carbazole. VI. On the Formation of N-Ethylcarbazoles in the Cadogan Reaction

Tsunashima, Yutaka,Kuroki, Masatane

, p. 315 - 318 (2007/10/02)

Reaction of 2',6-dimethyl-2-nitrobiphenyl with triethyl phosphite gave 4,5-dimethyl-9-ethylcarbazole besides 4,5-dimethylcarbazole.In this reaction, 4,5-dimethylcarbazole was ethylated by triethyl N-(2',6-dimethylbiphenyl-2-yl)phosphorimidate and diethyl N-(2',6-dimethylbiphenyl-2-yl)phosphoramidate, which arose from a nitrene-intermediate and triethyl phosphite.Analogous ethylations of carbazole with other phosphorimidate and phosphoramidates were investigated.

A nitrogen-15 nuclear magnetic resonance study of N-aryl phosphoramidates and phosphorimidates

Buchanan, G. W.,Morin, F. G.,Fraser, R. R.

, p. 2442 - 2446 (2007/10/02)

15N nuclear magnetic resonance chemical shifts and one-bond 15N-31P couplings are reported for a series of five N-arylphosphoramidates and four N-arylphosphorimidates.Results are interpreted in terms of an extensively delocalized N lone pair in the phosphoramidates, with p?-p? donation into the aromatic ring being dominant over p?-d? donation from nitrogen to phosphorus.

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