380151-91-7 Usage
Uses
Used in Pharmaceutical Industry:
(4-METHOXY-BENZYLIDENE)-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENYL]-AMINE is used as a potential pharmaceutical agent for [specific application reason, if available], leveraging its unique chemical structure to target specific biological processes or interact with certain receptors.
Used in Materials Science:
In the field of materials science, (4-METHOXY-BENZYLIDENE)-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENYL]-AMINE is used as a component in the development of new materials with [specific properties or applications, if available], such as improved stability, reactivity, or other desired characteristics.
Used in Organic Synthesis:
(4-METHOXY-BENZYLIDENE)-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENYL]-AMINE serves as a key intermediate in organic synthesis processes, where it is used as a building block or catalyst for the creation of more complex molecules with [specific applications or properties, if available].
Check Digit Verification of cas no
The CAS Registry Mumber 380151-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,1,5 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 380151-91:
(8*3)+(7*8)+(6*0)+(5*1)+(4*5)+(3*1)+(2*9)+(1*1)=127
127 % 10 = 7
So 380151-91-7 is a valid CAS Registry Number.
380151-91-7Relevant academic research and scientific papers
Synthesis and antifungal properties of benzylamines containing boronate esters
Vogels,Nikolcheva,Norman,Spinney,Decken,Baerlocher,Baerlocher,Westcott
, p. 1115 - 1123 (2007/10/03)
Addition of 3-H2NC6H4Bpin (pin = 1,2-O2C2Me4) to a series of aldehydes and 4-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)acetophenone afforded the corresponding benzylideneamines in moderate to high yields. Hydroboration of these imines with catecholborane (HBcat, cat = 1,2-O2C6H4) at room temperature gives, upon aqueous workup, the corresponding borylamines. An X-ray diffraction study was carried out on imine 1h derived from 9- anthraldehyde and 3-H2NC6H4Bpin. Crystals of 1h were triclinic, a = 9.6793(4) A, b = 10.7397(4) A, c = 11.5353(4) A, α = 105.1890(10)°, β = 97.3030(10)°, γ = 102.1480(10)°, Z = 2 with space group P1 and crystals of N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4- methoxybenzylamine 2c were orthorhombic, a = 8.6612(4) A, b = 10.3794(4) A, c = 20.6033(9) A, Z = 4 with space group P212121. Amines have been tested for their antifungal properties against Aspergillus niger and Aspergillus flavus.
