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Benzenemethanamine, N-[(diphenylphosphinyl)methyl]-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95107-72-5

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95107-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95107-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,1,0 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95107-72:
(7*9)+(6*5)+(5*1)+(4*0)+(3*7)+(2*7)+(1*2)=135
135 % 10 = 5
So 95107-72-5 is a valid CAS Registry Number.

95107-72-5Relevant academic research and scientific papers

Elaboration of the Benzazaphospholine Framework: a New Illustration of the Parham Protocol

Couture, Axel,Deniau, Eric,Grandclaudon, Pierre

, p. 1329 - 1330 (2007/10/02)

1-Alkyl-3-phenyl-1,3-benzazaphospholine oxides are efficiently prepared by Parham-type anionic cyclisation of ortho-lithiated N-alkyl-N-diphenylphosphinoylmethylaniline derivatives obtained by sequential treatment of the parent brominated compounds with methyllithium and tert-butyllithium.

Synthesis of indoles using (N-arylaminomethyl)diphenylphosphine oxides

Zorgdrager, Jan,Broekhof, Nico L. J. M.,Gen, Arne van der

, p. 441 - 444 (2007/10/02)

A new route for the synthesis of 1,3-disubstituted indoles, based on (N-arylaminomethyl)-diphenylphosphine oxide (1) chemistry, is described.Adducts 2, obtained by addition of the carbanions from 1 to aldehydes, were treated with p-toluenesulfonic acid to form the desired indoles 4 in good yields, without isolation of the intermediate amino ketones 3.

The synthesis of α-amino-substituted diphenylphosphine oxides

Broekhof, N. L. J. M.,Elburg, P. van,Gen, A. van der

, p. 312 - 316 (2007/10/02)

Four methods with differing but overlapping specificity are described for the synthesis of α-unsubstituted as well as α-substituted (aminomethyl)diphenylphosphine oxides.The first method is based on the Arbusov reaction, the second on a Mannich-type condensation of diphenylphosphine oxide with aldehydes and secondary amines, the third on the addition of Ph2P(O)H to enamines and the fourth on the reaction of anions derived from α-unsubstituted (aminomethyl)diphenylphosphine oxides with various electrophiles.

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