1283595-88-9 Usage
Uses
Used in Pharmaceutical Industry:
(E)-2-(4-methoxybenzylideneamino)-1-phenylethanol is used as an intermediate compound for the synthesis of other organic compounds, playing a crucial role in the development of pharmaceutical products. Its versatile chemical structure allows it to be a key component in creating a wide range of medications.
Used in Chemical Research:
In the field of chemical research, (E)-2-(4-methoxybenzylideneamino)-1-phenylethanol is utilized as a reagent. Its properties make it suitable for various experimental procedures and the investigation of new chemical reactions and processes.
Used as a Chiral Building Block:
(E)-2-(4-methoxybenzylideneamino)-1-phenylethanol is also recognized for its potential as a chiral building block in the production of biologically active compounds. Its unique structure contributes to the development of enantiomerically pure molecules, which are essential in the creation of more effective and selective drugs.
Used for Pharmacological Properties:
(E)-2-(4-methoxybenzylideneamino)-1-phenylethanol has been studied for its potential as an anti-inflammatory and anti-cancer agent. Its pharmacological properties make it a promising candidate for further research and development in the medical field, potentially leading to new treatments for various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1283595-88-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,3,5,9 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1283595-88:
(9*1)+(8*2)+(7*8)+(6*3)+(5*5)+(4*9)+(3*5)+(2*8)+(1*8)=199
199 % 10 = 9
So 1283595-88-9 is a valid CAS Registry Number.
1283595-88-9Relevant academic research and scientific papers
An effective method to prepare imines from aldehyde, bromide/epoxide, and aqueous ammonia
Huang, Jing-Mei,Zhang, Jue-Fei,Dong, Yi,Gong, Wen
supporting information; experimental part, p. 3511 - 3514 (2011/06/22)
A three-component reaction of aldehydes, alkyl bromides, and ammonia to form imines was studied. Aqueous ammonia was applied as the nitrogen source and solvent in the reaction. For the aromatic aldehyde, the product yields are good to excellent and the reaction conditions are mild to be compatible with a range of functional groups. The reaction of aldehydes and aqueous ammonia with epoxides was also studied and imines bearing a vicinal hydroxyl group can be obtained efficiently and regioselectively. And studies showed that this method allows the synthesis of primary amines and especially 1,2-amino alcohol selectively in high yield. It is proposed that the reaction pathway might involve a key intermediate of hydrobenzamide.
