76858-94-1 Usage
Description
1,2-Bis(dipentafluorophenylphosphino)ethane is a white to light yellow crystalline powder that serves as a crucial intermediate in the pharmaceutical industry and organic synthesis. Its unique chemical properties make it a valuable compound for various applications.
Uses
Used in Pharmaceutical Industry:
1,2-Bis(dipentafluorophenylphosphino)ethane is used as a pharmaceutical intermediate for the development of new drugs and therapeutic agents. Its chemical structure allows for the creation of complex molecules with specific properties, making it a versatile building block in the synthesis of various pharmaceutical compounds.
Used in Organic Syntheses:
In the field of organic chemistry, 1,2-Bis(dipentafluorophenylphosphino)ethane is used as an intermediate in the synthesis of a wide range of organic compounds. Its unique phosphino groups enable the formation of various chemical bonds, facilitating the creation of complex molecular structures with specific functionalities.
Overall, 1,2-Bis(dipentafluorophenylphosphino)ethane is a valuable compound in both the pharmaceutical and organic synthesis industries due to its unique chemical properties and its role as an intermediate in the development of new drugs and organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 76858-94-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,5 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76858-94:
(7*7)+(6*6)+(5*8)+(4*5)+(3*8)+(2*9)+(1*4)=191
191 % 10 = 1
So 76858-94-1 is a valid CAS Registry Number.
76858-94-1Relevant articles and documents
Stereospecific deoxygenation of phosphine oxides with retention of configuration using triphenylphosphine or triethyl phosphite as an oxygen acceptor
Wu, Hai-Chen,Yu, Jin-Quan,Spencer, Jonathan B.
, p. 4675 - 4678 (2007/10/03)
(Chemical Equation Presented) A new protocol for deoxygenation of various phosphine oxides with retention of configuration is described. The advantage of the new method includes milder conditions and considerably shortened reaction times. Mechanistic studies about the oxygen transfer between the starting phosphine oxide and the sacrificial triphenylphosphine are also presented.
The Preparation and Properties of Some Diposphines R2PCH2CH2PR2 (R = Alkyl or Aryl) and of their Rhenium(I) Dinitrogen Derivatives
Chatt, Joseph,Hussain, Wasif,Leigh, G. Jeffery,Ali, Hapipah Mohd.,Pickett, Christopher J.,Rankin, Douglas A.
, p. 1131 - 1136 (2007/10/02)
The synthesis of a range of diphosphines R2PCH2CH2PR2 from Cl2PCH2CH2PCl2 is described.The properties of a series of complexes derived from them are discussed.The relationship between the values of E1/2ox an