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W(CO)5PH(CH(Si(CH3)3)2)(NH(C6H5)) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1374585-29-1

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1374585-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374585-29-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,5,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1374585-29:
(9*1)+(8*3)+(7*7)+(6*4)+(5*5)+(4*8)+(3*5)+(2*2)+(1*9)=191
191 % 10 = 1
So 1374585-29-1 is a valid CAS Registry Number.

1374585-29-1Downstream Products

1374585-29-1Relevant academic research and scientific papers

Synthesis of aminophosphane complexes: Searching the boundary between phosphanide and phosphinidenoid complex chemistry

Duan, Lili,Schnakenburg, Gregor,Daniels, Joerg,Streubel, Rainer

, p. 2314 - 2319 (2012/06/18)

Aminophosphane complexes 3a-e have been prepared by two different pathways: (1) the thermal reaction of 2H-azaphosphirene complex 1 with primary or secondary amine derivatives at 75 °C (3a,b,d,e) or (2) the reaction of chlorophosphane complex 2 with sodium diphenylamide (3c). In the latter case, complex 3c was obtained together with the diphosphene complex 6, thus providing evidence for the transient formation of Na/X phosphinidenoid complexes 4a,b and/or the terminal phosphinidene complex 5. Preliminary deprotonation studies, carried out on complex 3a by using lithium diisopropylamide in TMEDA in the presence of 12-crown-4 at low temperature, yielded a mixture of the Li/NMe 2 phosphinidenoid complex 7 together with the nonligated phosphane derivative 8, which could not be separated. Complexes 3a,b,d,e and 6 were characterized by NMR and IR spectroscopy, MS, and elemental analysis. The structures of complexes 3c-e and 6 were confirmed by single-crystal X-ray diffraction analysis. Aminophosphane complexes 3a-e have been prepared by two routes. Complex 3c was obtained along with diphosphene complex 6, giving evidence for the formation of transient Na/X phosphinidenoid complexes 4a,b and/or phosphinidene complex 5. Initial studies on the deprotonation of 3a led to the formation of the Li/NMe2 phosphinidenoid complex 7a along with the nonligated phosphane derivative 8. Copyright

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