3968-92-1 Usage
Uses
Used in Organic Chemistry:
(2-Butyl)triphenylphosphonium Bromide is used as a nucleophile and reducing agent for facilitating the synthesis of complex organic molecules. Its strong nucleophilic nature allows it to participate in various chemical reactions, making it a valuable component in the construction of intricate molecular structures.
Used in Synthetic Chemistry:
In the field of synthetic chemistry, (2-Butyl)triphenylphosphonium Bromide is utilized as a key reagent in the synthesis of a wide range of organic compounds. Its ability to act as a strong nucleophile and a reducing agent is crucial for achieving the desired transformations in target molecules.
Used in Wittig Reactions:
(2-Butyl)triphenylphosphonium Bromide is employed as a reagent in Wittig reactions, which are widely used for the construction of carbon-carbon double bonds. Its role in these reactions is to provide a stable and reactive source of a phosphonium ylide, which is essential for the formation of the desired double bond.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its applications in organic and synthetic chemistry, (2-Butyl)triphenylphosphonium Bromide may also be used in the pharmaceutical industry for the synthesis of complex drug molecules. Its ability to facilitate the formation of carbon-carbon double bonds can be particularly useful in the development of novel therapeutic agents.
Used in Research and Development:
In research and development settings, (2-Butyl)triphenylphosphonium Bromide is used as a tool to explore new synthetic pathways and develop innovative chemical reactions. Its unique properties make it a valuable asset in the pursuit of new chemical knowledge and the creation of advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 3968-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,6 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3968-92:
(6*3)+(5*9)+(4*6)+(3*8)+(2*9)+(1*2)=131
131 % 10 = 1
So 3968-92-1 is a valid CAS Registry Number.
InChI:InChI=1/C22H24P.BrH/c1-3-19(2)23(20-13-7-4-8-14-20,21-15-9-5-10-16-21)22-17-11-6-12-18-22;/h4-19H,3H2,1-2H3;1H/q+1;/p-1
3968-92-1Relevant academic research and scientific papers
Studies on the intramolecular electron transfer catalyzed thermolysis of 1,2-dioxetanes
Nery, Ana L. P.,Wei?, Dieter,Catalani, Luiz H.,Baader, Wilhelm J.
, p. 5317 - 5327 (2007/10/03)
This work reports the synthesis and the chemiluminescence properties of the dioxetanes: 4-ethyl-4-methyl-3-(3-methoxyphenyl)-1,2-dioxetane (I), 4-ethyl-4-methyl-3-(3-tert-butyldimethylsilyloxyphenyl)-1,2-dioxetane (II), 4,4-dimethyl-3-(3-methoxybenzyl)-1,2-dioxetane (III) and 4,4-dimethyl-3-(3-tert-butyldimethylsilyloxybenzyl)-1,2-dioxetane (IV). While in the thermal decomposition of I-IV preferential formation of triplet excited states is observed, in the presence of fluoride ions the decomposition rate constants of II and IV increase drastically and singlet excited states are formed with high quantum yields. These results are discussed based on the CIEEL ('Chemically Initiated Electron Exchange Luminescence') mechanism where the decomposition of the dioxetanes should be initiated by an intramolecular electron transfer from the phenolate ion (generated by fluoride catalyzed deprotection of the silyloxy group), either directly bound to the peroxidic ring (II) or separated from it by a methylene bridge (IV). (C) 2000 Elsevier Science Ltd.
