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(N,N-dimethyl)-(chloro-phenyl-phosphino)-amine, also known as chlorophenyl-N,N-dimethylphosphinamine, is an organophosphorus compound characterized by a phosphorus atom bonded to a chlorophenyl group and two methyl groups. This chemical is a versatile reagent in organic synthesis, particularly in the formation of phosphorus-containing compounds. It is used as a ligand in transition metal catalysis and as a precursor in the synthesis of various phosphorus-based compounds. The compound is sensitive to moisture and air, and it is typically handled under an inert atmosphere to prevent degradation. Its applications span across pharmaceuticals, agrochemicals, and materials science, where it contributes to the development of new molecules with unique properties.

4073-30-7

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4073-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4073-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4073-30:
(6*4)+(5*0)+(4*7)+(3*3)+(2*3)+(1*0)=67
67 % 10 = 7
So 4073-30-7 is a valid CAS Registry Number.

4073-30-7 Well-known Company Product Price

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  • Aldrich

  • (771120)  Dimethylaminophenylchlorophosphine  95%

  • 4073-30-7

  • 771120-500MG

  • 923.13CNY

  • Detail

  • Aldrich

  • (771120)  Dimethylaminophenylchlorophosphine  95%

  • 4073-30-7

  • 771120-2G

  • 2,999.88CNY

  • Detail

4073-30-7Relevant academic research and scientific papers

A flexible, highly efficient method for the preparation of homochiral oxazaphospholidine-boranes

Sheehan, Susan Kult,Jiang, Meiqun,McKinstry, Lydia,Livinghouse, Tom,Garton, Donna

, p. 6155 - 6162 (2007/10/02)

An efficient and operationally simple procedure for the synthesis of 2-substituted 3,4-dimethyl-5-phenyloxazaphospholidine derivatives has been developed. This new method permits the large scale preparation of a range of electronically and sterically diff

PHOSPHA-S-TRIAZINES. VII. PHENYL-BRIDGED PHOSPHA-S-TRIAZINES

Paciorek, K. J. L.,Ito, T. I.,Nakahara, J. H.,Harris, D. H.,Kratzer, R. H.

, p. 185 - 198 (2007/10/02)

1,2-Bis(phenyltrichlorophosphino)benzene was synthesized by a 4-step process in an overall 58percent yield.Interaction of the bis(trichlorophosphorane) with the appropriate imidoylamidines afforded the novel 1,4-bisbenzene and 1,4-bisbenzene.Electron impact fragmentation patterns of these compounds could be correlated with those of the single ring analogues.The thermal and thermal oxidative stability of the phenyl-bridged dumbbells was lower than that of the corresponding monomeric mono- and diphospha-s-triazines.These materials were found to be effective in arresting the degradation of perfluoroalkylether fluids in oxidizing atmospheres in the presence of metals.

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