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(η1-2,3-diphenyl-1-(9-fluorenyl)phosphirene-P)pentacarbonyltungsten is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115076-40-9

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115076-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115076-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,7 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115076-40:
(8*1)+(7*1)+(6*5)+(5*0)+(4*7)+(3*6)+(2*4)+(1*0)=99
99 % 10 = 9
So 115076-40-9 is a valid CAS Registry Number.

115076-40-9Downstream Products

115076-40-9Relevant academic research and scientific papers

Introducing new phosphorus substituents in terminal phosphinidene complexes. An illustration with [(ethoxycarbonyl)phosphinidene]-, (tert-butoxyphosphinidene)-, and (fluorenylphosphinidene)pentacarbonyltungsten complexes

Holand, Serge,Mathey, Fran?ois

, p. 1796 - 1801 (1988)

The reaction of ethyl chloroformate with the [(3,4-dimethylphospholyl)lithium(P-W)]pentacarbonyltungsten complex yields the corresponding 1-(ethoxycarbonyl)phosphole complex. Upon reaction with dimethyl acetylenedicarboxylate, this phosphole derivative gives the corresponding 7-phosphanorbornadiene complex which in turn appears to be a good precursor for the transient (ethoxycarbonyl)phosphimdene complex [EtO-C(O)-P=W(CO)5]. This transient species cleanly reacts with methanol, diethylamme, and tolan to give the expected phosphinite and phosphirene complexes. However, it appears impossible to perform the P-CO2Et → P-H conversion via the attack of OH- at the carbonyl group without destroying the phosphinite and phosphirene structures. Thus [EtO-C(O)-P=W(CO)5] cannot be used as a masked [HP=W(CO)5]. In order to vary the substituent at phosphorus in the transient phosphimdene complexes, it is possible to start with 1-cyano-3,4-dimethylphosphole which is easily obtained from BrCN and the appropriate phospholyl anion. This 1-cyanophosphole provides for the first time an easy access to 1-alkoxy-, 1-amino- 1-aryl-, and 1-alkynyl-3,4-dimethylphospholes. Using the same basic scheme as with the ethoxycarbonyl substituent, it is possible to prepare from these new phospholes the corresponding 7-phoephanorbornadiene complexes. The precursors of [t-BuO-P=W(CO)5] and [9-fluorenyl-P=W(CO)5] are thus prepared and tested as an example.

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