436088-69-6 Usage
Description
(4-ISOPROPYL-BENZYL)-(4-METHOXY-BENZYL)-AMINE is a chemical compound belonging to the class of amines, characterized by the presence of both isopropyl and methoxybenzyl groups. It is recognized for its unique chemical structure and reactivity, which allows it to modify the properties of other organic molecules. This characteristic makes it a valuable building block in organic synthesis and pharmaceutical research for the development of various compounds.
Uses
Used in Pharmaceutical Research:
(4-ISOPROPYL-BENZYL)-(4-METHOXY-BENZYL)-AMINE is used as a building block for the development of pharmaceuticals due to its ability to modify the properties of other organic molecules. Its unique structure and reactivity contribute to the synthesis of a wide range of organic compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (4-ISOPROPYL-BENZYL)-(4-METHOXY-BENZYL)-AMINE is used as a key component for creating various specialized chemicals. Its versatility in modifying the properties of other molecules makes it an essential tool in the production of a diverse array of chemical products.
Used in Chemical Production:
(4-ISOPROPYL-BENZYL)-(4-METHOXY-BENZYL)-AMINE is also utilized in the chemical production industry as a vital component in the synthesis of a broad spectrum of organic compounds. Its unique chemical structure plays a crucial role in enhancing the properties of these compounds, making them suitable for various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 436088-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,0,8 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 436088-69:
(8*4)+(7*3)+(6*6)+(5*0)+(4*8)+(3*8)+(2*6)+(1*9)=166
166 % 10 = 6
So 436088-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H23NO/c1-14(2)17-8-4-15(5-9-17)12-19-13-16-6-10-18(20-3)11-7-16/h4-11,14,19H,12-13H2,1-3H3/p+1
436088-69-6Relevant articles and documents
Synthesis and evaluation of Zn(II) dithiocarbamate complexes as potential antibacterial, antibiofilm, and antitumor agents
Maurya, Vinay Kumar,Singh, Ashish Kumar,Singh, Ravi Pratap,Yadav, Shivangi,Kumar, Krishna,Prakash, Pradyot,Prasad, Lal Bahadur
, p. 3338 - 3358 (2019/11/26)
Four complexes having the formula [Zn(L)2] [L1 = (C18H20NS2 –), N-(4-isopropyl-benzyl)-(benzyl)-dithiocarbamate], [L2 = (C10H12NS2 –), N-(benzyl)-(ethyl)-dithiocarbamate], [L3 = (C19H22ONS2 –), N-(4-isopropyl-benzyl)-(4-methoxy-benzyl)-dithiocarbamate], and [L4 = (C16H16NS2 –), N-(benzyl)-(4-methyl-benzyl)-dithiocarbamate] have been contemplated, synthesized, and characterized by elemental analysis and IR, 1H, 13C NMR and UV–visible absorption spectra. All Zn(II) complexes have similar geometry and coordination number. Complex A2 (with ligand L2) crystallizes in triclinic system with space group P-1 having distorted square pyramidal geometry which was stabilized by weak C–H···π and C–H···S intramolecular interactions. The antibacterial, antibiofilm, and antitumor activities of the complexes have been screened and A2 and A3 showed their prominence. Interestingly, both A2 and A3 showed more killing potential against multi-drug resistant gram-positive isolates with MIC indices of 16 μg mL?1 and 16 μg mL?1, respectively, against both MRSA and MSSA, while the antitumor agent A3 showed its prominence with GI50 and LC50 41.15 and 133.73 μg mL?1, respectively.
