51549-86-1 Usage
Uses
Used in Organic Synthesis:
Buta-2,3-dien-2-ylcyclopropane is utilized as a synthetic intermediate for the creation of various organic compounds. Its unique structure allows for a range of reactions, such as ring-opening and addition reactions, which can be harnessed to produce complex organic molecules with potential applications in pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, buta-2,3-dien-2-ylcyclopropane serves as a key intermediate in the synthesis of specific drug molecules. Its reactivity and structural features facilitate the development of novel compounds with therapeutic potential, contributing to the discovery of new medications for various diseases and conditions.
Used in Agrochemical Development:
Buta-2,3-dien-2-ylcyclopropane is also employed in the agrochemical sector as a precursor for the synthesis of pesticides and other crop protection agents. Its ability to participate in various chemical reactions enables the production of effective and targeted agrochemicals that can protect crops from pests and diseases.
Used in Materials Science:
In the field of materials science, buta-2,3-dien-2-ylcyclopropane is used as a component in the development of new materials with specialized properties. Its incorporation into polymers and other materials can lead to the creation of substances with unique characteristics, such as enhanced strength, flexibility, or chemical resistance, which can be applied in various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 51549-86-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,4 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51549-86:
(7*5)+(6*1)+(5*5)+(4*4)+(3*9)+(2*8)+(1*6)=131
131 % 10 = 1
So 51549-86-1 is a valid CAS Registry Number.
51549-86-1Relevant academic research and scientific papers
Polylithiumorganic compounds. Part 28. The reaction of allene and alkyl substituted allenes with lithium metal
Maercker, Adalbert,Tatai, Andrea,Grebe, Burkhard,Girreser, Ulrich
, p. 1 - 8 (2007/10/03)
The reaction of allene (3a) and alkyl substituted allenes 1,2-hexadiene (3b), cyclopropylallene (3c), and vinylidene cyclopropane (3d) with lithium metal was investigated in order to access 2,3-dilithioalkenes 4a-d. These dilithioalkenes 4a-d are very reactive in polar solvents like THF and act as strong bases, either metalation of the starting allene 3a-d, the solvent, or sufficiently acidic intermediates like 8 a-d is observed. The metalation products 5-7 show follow-up reactions like 1,3-H shift to the corresponding 1-lithio-1-alkynes 8 and subsequent metalation to the dilithioalkynes 9. Additionally, lithium hydride elimination and ring-chain rearrangement (for 5c) are observed. 1,2-Hexadiene (3b) can be brought to reaction with lithium metal in the apolar solvent pentane, here the follow-up reactions are much slower due to the insolubility of 4b. In all cases the elucidation of the reaction pathways is hampered by the formation of complex mixtures of, amongst others, regio- and stereoisomeric products upon quenching with simple electrophiles.
