173948-30-6 Usage
Description
(E)-N,N-diisopropyl-3-phenylprop-2-en-1-amine, with the molecular formula C17H27N, is a chemical compound that belongs to the class of tertiary amines and alkenes. It is characterized by a unique arrangement of isopropyl and phenyl groups attached to the amine nitrogen. (E)-N,N-diisopropyl-3-phenylprop-2-en-1-amine is known for its versatile reactivity and structural features, making it a valuable asset in the field of chemistry.
Uses
Used in Organic Synthesis:
(E)-N,N-diisopropyl-3-phenylprop-2-en-1-amine is used as a ligand or catalyst in organic synthesis, facilitating various chemical reactions and improving their efficiency. Its unique structural features allow it to interact with a wide range of substrates, making it a valuable tool in the development of new chemical processes.
Used in Pharmaceutical and Agrochemical Compounds:
(E)-N,N-diisopropyl-3-phenylprop-2-en-1-amine serves as a building block in the preparation of various pharmaceutical and agrochemical compounds. Its structural diversity and reactivity enable the creation of novel molecules with potential therapeutic or pesticidal properties.
Used in Medicinal Chemistry and Drug Discovery:
(E)-N,N-diisopropyl-3-phenylprop-2-en-1-amine has potential applications in medicinal chemistry and drug discovery due to its structural features and versatile reactivity. Researchers can leverage these properties to design and synthesize new drug candidates with improved pharmacological profiles.
Used in Research and Industrial Applications:
(E)-N,N-diisopropyl-3-phenylprop-2-en-1-amine plays a significant role in both research and industrial applications within the field of chemistry. Its unique properties and reactivity make it an essential component in the development of new chemical processes, materials, and products.
Check Digit Verification of cas no
The CAS Registry Mumber 173948-30-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,9,4 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 173948-30:
(8*1)+(7*7)+(6*3)+(5*9)+(4*4)+(3*8)+(2*3)+(1*0)=166
166 % 10 = 6
So 173948-30-6 is a valid CAS Registry Number.
173948-30-6Relevant articles and documents
Palladium-Catalyzed Allylic Amination of Allylic Alcohols with Tin(II) Chloride and Triethylamine
Masuyama, Yoshiro,Kagawa, Masaaki,Kurusu, Yasuhiko
, p. 1121 - 1122 (1995)
Allylic alcohols caused allylic amination with primary or secondary amines in the presence of a catalytic amount of Pd(PPh3)4 and stoichiometric amount of tin(II) chloride in THF at 50 deg C to produce the corresponding allylic amines regioselectively.
C-N Bond Formation from Allylic Alcohols via Cooperative Nickel and Titanium Catalysis
Nazari, S. Hadi,Tiempos-Flores, Norma,Forson, Kelton G.,Bourdeau, Jefferson E.,Michaelis, David J.
, p. 10646 - 10654 (2018/09/06)
Amination of allylic alcohols is facilitated via cooperative catalysis. Catalytic Ti(O-i-Pr)4 is shown to dramatically increase the rate of nickel-catalyzed allylic amination, and mechanistic experiments confirm activation of the allylic alcohol by titanium. Aminations of primary and secondary allylic alcohols are demonstrated with a variety of amine nucleophiles. Diene-containing substrates also cyclize onto the nickel allyl intermediate prior to amination, generating carbocyclic amine products. This tandem process is only achieved under our cooperative catalytic system.
Anti-Markovnikov rearrangement in sulfur mediated allylic C-H amination of olefins
Zhang, Zhong,Du, Hongguang,Xu, Jiaxi,Li, Pingfan
supporting information, p. 11547 - 11550 (2016/10/03)
Cationic rearrangement reactions usually follow Markovnikov's rule to give more substituted carbocations as stable intermediates. During our study on sulfur mediated allylic C-H amination of olefins, very rare cases of anti-Markovnikov rearrangement from secondary carbocations toward primary carbocations or primary triflates were observed.
