173416-01-8 Usage
Description
(1-FURAN-2-YL-BUT-3-ENYL)-(4-METHOXY-PHENYL)-AMINE, also known as 2-amino-1-((furan-2-yl)ethyl)-5-(4-methoxyphenyl)pent-4-en-1-one, is a chemical compound with the molecular formula C18H19NO2. It belongs to the class of aromatic amines and contains a furan ring, a butenyl group, and a methoxyphenyl group. (1-FURAN-2-YL-BUT-3-ENYL)-(4-METHOXY-PHENYL)-AMINE is commonly used in organic synthesis and pharmaceutical research for its potential biological activities. Due to its structural and functional properties, it may have applications in the development of novel drugs and pharmacological agents. Further research and studies may be required to fully understand the potential uses and effects of this chemical compound.
Uses
Used in Pharmaceutical Research:
(1-FURAN-2-YL-BUT-3-ENYL)-(4-METHOXY-PHENYL)-AMINE is used as a research compound for exploring its potential biological activities and applications in the development of novel drugs and pharmacological agents. Its unique structure, which includes a furan ring, a butenyl group, and a methoxyphenyl group, may contribute to its potential as a therapeutic agent.
Used in Organic Synthesis:
In the field of organic synthesis, (1-FURAN-2-YL-BUT-3-ENYL)-(4-METHOXY-PHENYL)-AMINE serves as a key intermediate or building block in the synthesis of more complex organic molecules. Its presence in various chemical reactions can lead to the formation of new compounds with diverse applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 173416-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,4,1 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 173416-01:
(8*1)+(7*7)+(6*3)+(5*4)+(4*1)+(3*6)+(2*0)+(1*1)=118
118 % 10 = 8
So 173416-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H17NO2/c1-3-5-14(15-6-4-11-18-15)16-12-7-9-13(17-2)10-8-12/h3-4,6-11,14,16H,1,5H2,2H3
173416-01-8Relevant articles and documents
Asymmetric Petasis Borono-Mannich Allylation Reactions Catalyzed by Chiral Biphenols
Jiang, Yao,Schaus, Scott E.
, p. 1544 - 1548 (2017/02/05)
Chiral biphenols catalyze the asymmetric Petasis borono-Mannich allylation of aldehydes and amines through the use of a bench-stable allyldioxaborolane. The reaction proceeds via a two-step, one-pot process and requires 2–8 mole % of 3,3′-Ph2-BINOL as the optimal catalyst. Under microwave heating the reaction affords chiral homoallylic amines in excellent yields (up to 99 %) and high enantioselectivies (er up to 99:1). The catalytic reaction is a true multicomponent condensation reaction whereas both the aldehyde and the amine can possess a wide range of structural and electronic properties. Use of crotyldioxaborolane in the reaction results in stereodivergent products with anti- and syn-diastereomers both in good diastereoselectivities and enantioselectivities from the corresponding E- and Z-borolane stereoisomers.
Palladium-catalyzed, one-pot, three-component synthesis of homoallylic amines from aldehydes, anisidine, and allyl trifluoroacetate
Grote, Robin E.,Jarvo, Elizabeth R.
supporting information; experimental part, p. 485 - 488 (2009/07/18)
(Chemical Equation Presented) An allylation reaction that generates homoallylic amines using allyl trifluoroacetate as a nucleophilic allylmetal precursor is reported. A palladium complex catalyzes two transformations in one pot: formation of allylsilane
Palladium-catalyzed allylation of imines with allyl alcohols
Shimizu, Masamichi,Kimura, Masanari,Watanabe, Toshiya,Tamaru, Yoshinao
, p. 637 - 640 (2007/10/03)
(Chemical Equation Presented) A catalytic system, Pd(OAc)2 (10 mol %)-P(n-Bu)3 (20 mol %)-Et3B (360 mol %), promotes allylic alcohols to undergo the allylation of anisidineimines of aromatic and aliphatic aldehydes and furnishes homoallylamines in good to moderate yields. The reaction shows unique stereoselectivity, giving anti-isomers selectively.
