55795-18-1 Usage
Uses
Used in Organic Synthesis:
(E)-1-Butadienylphosphonium Bromide is used as a reagent for the production of various organic compounds. Its unique structure allows for a wide range of reactions, making it a valuable tool in the synthesis of complex organic molecules.
Used in Polymer Synthesis:
In the polymer industry, (E)-1-Butadienylphosphonium Bromide is utilized as a catalyst to facilitate the synthesis of polymers. Its catalytic properties enable the production of polymers with specific characteristics, tailored to various applications.
Used in Research Laboratories:
(E)-1-Butadienylphosphonium Bromide is employed in research settings for the study of phosphonium chemistry. It serves as a model compound to explore the properties and potential applications of phosphonium compounds in different fields, including material science, pharmaceuticals, and chemical engineering.
Used as a Precursor:
(E)-1-Butadienylphosphonium Bromide is also used as a precursor in the preparation of other phosphorus-containing compounds. Its reactivity and structural features make it a suitable starting material for the synthesis of a variety of phosphorus-based molecules with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 55795-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,9 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55795-18:
(7*5)+(6*5)+(5*7)+(4*9)+(3*5)+(2*1)+(1*8)=161
161 % 10 = 1
So 55795-18-1 is a valid CAS Registry Number.
55795-18-1Relevant academic research and scientific papers
Synthesis of 1,3-dienes of (E,Z) configuration by a three-component coupling strategy
White, James D.,Jensen, Mark S.
, p. 5743 - 5756 (2007/10/02)
Three-component coupling of an anionic nucleophile, butadienyltriphenylphosphonium bromide, and an aldehyde gave conjugated dienes of predominantly (E,Z) configuration. Dianions of β-dicarbonyl systems and dicarboxylic acids, and monoanions of sulfones we
Total Synthesis of (+)-Latrunculin A, an Ichthyotoxic Metabolite of the Sponge Latrunculia magnifica, and Its C-15 Epimer
White, James D.,Kawasaki, Motoji
, p. 5292 - 5300 (2007/10/02)
Latrunculin A (1), an ichthyotoxic metabolite of the sponge Latrunculia magnifica with potent inhibitory action on microfilament-mediated processes involved in cell division, was synthesized via a convergent approach.Construction of a major segment of the latrunculin backbone was accomplished by means of a three-component coupling of aldehyde 24, β-keto ester 27, and phosphonium salt 26, which established the conjugated E,Z-diene moiety of 31.The thiazolidinone subunit of 1 was elaborated in the form of 39 from L-cysteine and was linked to 35 without nitrogen protection.Final lactonization of 47 was carried out using the Mitsunobu protocol.A parallel sequence employing the epimeric seco acid 48 produced 15-epilatrunculin A.
