893591-54-3 Usage
Uses
Used in Pharmaceutical Industry:
[(3-chlorophenyl)methyl](prop-2-en-1-yl)amine is used as an intermediate for the synthesis of various organic compounds, playing a crucial role in the development of new pharmaceutical products. Its unique structure, which includes a chlorine atom and multiple reactive groups, allows for a wide range of chemical modifications and the creation of diverse molecules with potential therapeutic applications.
Used in Organic Reactions:
[(3-chlorophenyl)methyl](prop-2-en-1-yl)amine also serves as a reagent in organic reactions, facilitating the formation of new chemical bonds and contributing to the synthesis of complex molecules. Its presence can enhance the efficiency and selectivity of these reactions, making it a valuable tool in the field of organic chemistry.
Used in Building Complex Molecules:
The versatility of [(3-chlorophenyl)methyl](prop-2-en-1-yl)amine, stemming from its phenyl and prop-2-en-1-yl groups, makes it an ideal building block for the preparation of complex molecules. These complex molecules can be utilized in various applications, including the development of new drugs, materials, and other advanced chemical products.
Caution:
It is important to handle and use [(3-chlorophenyl)methyl](prop-2-en-1-yl)amine with care, as it may possess potential hazards and toxicity. Proper safety measures and precautions should be taken to minimize risks during its use in research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 893591-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,5,9 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 893591-54:
(8*8)+(7*9)+(6*3)+(5*5)+(4*9)+(3*1)+(2*5)+(1*4)=223
223 % 10 = 3
So 893591-54-3 is a valid CAS Registry Number.
893591-54-3Relevant articles and documents
Selective hydrosilylation of N-allylimines using a (3-iminophosphine)palladium precatalyst
Tafazolian, Hosein,Schmidt, Joseph A.R.
, p. 685 - 689 (2016/02/18)
Hydrosilylation utilizing a (3-iminophosphine)palladium catalyst leads to the selective reduction of the imine unit of allylimines. Successful reduction of twenty-five different substituted aromatic and alkyl allylimines demonstrated the scope and selecti
Ring-closing metathesis of vinyl fluorides towards α-fluorinated α,β-unsaturated lactams and lactones
Marhold, Michael,Stillig, Christian,Fr?hlich, Roland,Haufe, Günter
supporting information, p. 5777 - 5785 (2014/10/15)
Ring-closing olefin metathesis reactions (RCM) using Grubbs II or Hoveyda's catalysts have been applied to a series of N-alkenyl-N-benzyl-α-fluoroacrylamides. α-Fluoro-α,β-unsaturated γ- or δ-lactams incorporating a fluorinated double bond were obtained in moderate to good yields, depending on the nature of substituents on the benzyl ring. The corresponding seven- and eight-membered lactams were not formed under similar conditions. When the N-benzyl group was replaced by an N-tosyl group, the corresponding ε-lactam was also formed in 38% yield. When N-(2-fluoroallyl) derivatives were used instead of fluoroacryloyl derivatives, six-, seven-, and eight-membered N-heterocycles were obtained in low yields. This method was also used to synthesize fluorinated α,β-unsaturated analogues of pyrrolizidine and indolizidine alkaloids from prolinol, and also to synthesize N-benzyl-3-fluoroquinolone in three steps from commercially available 2-vinylaniline in 44% overall yield. Also 3-fluorocoumarin and 3-fluorochromene were prepared from ovinylphenol, and 3-fluoro-benzoxepine was available from o-allylphenol.
