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380151-91-7

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380151-91-7 Usage

Description

(4-METHOXY-BENZYLIDENE)-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENYL]-AMINE is a complex organic chemical compound characterized by the presence of a benzylidene group attached to an amine group and a dioxaborolan-2-yl group. The incorporation of methoxy and tetramethyl groups adds to the compound's unique structure and properties. (4-METHOXY-BENZYLIDENE)-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENYL]-AMINE holds potential for applications in pharmaceuticals, materials science, and organic synthesis, although further research and testing are required to confirm its specific uses and benefits. Careful handling is advised due to its complex nature and possible hazardous properties.

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.

380151-91-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H51129)  3-(4-Methoxybenzylideneamino)benzeneboronic acid pinacol ester   

  • 380151-91-7

  • 1g

  • 237.0CNY

  • Detail
  • Alfa Aesar

  • (H51129)  3-(4-Methoxybenzylideneamino)benzeneboronic acid pinacol ester   

  • 380151-91-7

  • 5g

  • 907.0CNY

  • Detail
  • Alfa Aesar

  • (H51129)  3-(4-Methoxybenzylideneamino)benzeneboronic acid pinacol ester   

  • 380151-91-7

  • 25g

  • 3675.0CNY

  • Detail

380151-91-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methoxyphenyl)-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanimine

1.2 Other means of identification

Product number -
Other names (E)-N-(4-Methoxybenzylidene)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:380151-91-7 SDS

380151-91-7Relevant articles and documents

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.

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