1834-01-1 Usage
Uses
Used in Chemical Synthesis:
Tributyl(2-ethoxy-2-oxoethyl)phosphonium is used as a reactant in the synthesis of organic compounds, contributing to the formation of various chemical products due to its reactivity and stability.
Used as a Solvent in Chemical Processes:
In the chemical industry, tributyl(2-ethoxy-2-oxoethyl)phosphonium is utilized as a solvent for its unique properties, including high thermal stability and low volatility, which make it suitable for a range of chemical processes.
Used in Pharmaceutical Industry:
Tributyl(2-ethoxy-2-oxoethyl)phosphonium is being studied for its potential applications in the pharmaceutical industry, where its unique properties may contribute to the development of new drugs or drug delivery systems.
Used in Agricultural Industry:
tributyl(2-ethoxy-2-oxoethyl)phosphonium is also being explored for its potential use in the agricultural sector, where it could be employed in the development of new agrochemicals or as a component in agricultural formulations to enhance crop protection or yield.
Check Digit Verification of cas no
The CAS Registry Mumber 1834-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1834-01:
(6*1)+(5*8)+(4*3)+(3*4)+(2*0)+(1*1)=71
71 % 10 = 1
So 1834-01-1 is a valid CAS Registry Number.
1834-01-1Relevant academic research and scientific papers
Stereocontrolled synthesis of the C21-C38 fragment of the unnatural enantiomer of the antibiotic nystatin A1.
Berkenbusch, Thilo,Brueckner, Reinhard
, p. 1545 - 1557 (2007/10/03)
The C(21)-C(38) fragment all-trans-41 of the unnatural enantiomer 1 of nystatin A(1) was prepared starting from the N-propionyl oxazolidinone 9. Aldol adduct ent-8 (ee > 96 %) derived in two steps was hydroborated with (thexyl)BH(2). Oxidative work-up and treatment with acid furnished delta-lactone 4. It contains the complete stereotetrade of the target molecule. The alpha,beta-unsaturated ester 28 was reached after another four steps. It should be a precursor for the polyene moieties of a variety of polyol,polyene macrolides. Illustrating that, the alpha,beta-unsaturated aldehyde 29 obtained from 28 and DIBAL was extended by 10 C atoms in four steps yielding the C(21)-C(38) segment 41. The latter set of transformations included the regio- and stereoselective Claisen rearrangement 32-->35.
