52032-55-0 Usage
Uses
Used in Organic Synthesis:
[4-(2-formylphenoxy)butyl](triphenyl)phosphonium is used as a reactant in organic synthesis for its ability to participate in various types of reactions, such as Wittig-type reactions and C-C bond formation. Its unique structure allows for the creation of a wide range of complex organic molecules.
Used in Drug Delivery Systems:
In the pharmaceutical industry, [4-(2-formylphenoxy)butyl](triphenyl)phosphonium is used as a component in drug delivery systems. Its properties make it a promising candidate for enhancing the delivery, bioavailability, and therapeutic outcomes of various drugs.
Used as an Antibacterial Agent:
[4-(2-formylphenoxy)butyl](triphenyl)phosphonium is also studied for its potential use as a phosphonium salt with antibacterial properties. Its ability to combat bacterial infections makes it a valuable asset in the development of new antimicrobial agents.
Check Digit Verification of cas no
The CAS Registry Mumber 52032-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,3 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52032-55:
(7*5)+(6*2)+(5*0)+(4*3)+(3*2)+(2*5)+(1*5)=80
80 % 10 = 0
So 52032-55-0 is a valid CAS Registry Number.
52032-55-0Relevant articles and documents
The adverse effect of benzannelation on the aromaticity of oxocinyl anion: A combined experimental and theoretical study
Kasmai, Hamid S.,Wang, Xiaodong,Doan, Hanh-Nhon,Femia, Josef F.,Yablonsky, Thad M.,Read, Mary E.,Dutton, David T.
, p. 1532 - 1544 (2010)
A synthesis of 2H-1-benzoxocin from readily available compounds was accomplished. The potentially 'aromatic' π-excessive systems 2H-1-benzoxocinyl and 6H-dibenz[b,f]oxocinyl anions were generated from their corresponding conjugate acid precursors 7c and 8, respectively. It was found that 2H-1-benzoxocinide 3d lacks the type of π-frame stability associated with the parent 2H-oxocinide 1d and that the dibenzo analog 5b is more unstable than 3d. Both 3d and 5b undergo rapid structural reorganization to form their corresponding stable isomeric anions. We were able to characterize the proton-quenched products of these anions as the ring-opened structures 15 and 18, respectively. 1H-NMR and an ab initio calculation at the 6-31g* level indicated that, unlike the 'aromatic' parent 2H-oxocinide 1d and the aza analog 3c, 3d incorporates a non-planar oxocinyl ring in which the negative charge is primarily localized on the pentadienyl moiety of the ring, but also partial delocalization of π-electron density onto the benzene ring occurs.
